E1b1a
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E1b1a
Haplogroup E-V38 is a human Y-chromosome DNA haplogroup. It is primarily distributed in Sub Saharan Africa. E-V38 has two basal branches, E-M329 (formerly E1b1c or E1b1*) and E-M2 (formerly E3a & E1b1a). The E-M329 subclade is today almost exclusively found in Ethiopia. E-M2 is the predominant subclade in Western Africa, Central Africa, Southern Africa and the region of African Great Lakes, and occurs at only moderate frequencies in some parts of North Africa, West Asia and Southern Europe. Origins The discovery of two SNPs (V38 and V100) by Trombetta et al. (2011) significantly redefined the E-V38 phylogenetic tree. This led the authors to suggest that E-V38 may have originated in East Africa. V38 joins the West African-affiliated E-M2 and the northern East African-affiliated E-M329 with an earlier common ancestor who, like E-P2, may have also originated in East Africa. The downstreams SNP E-M180 may have originated on the moist south-central Saharan savannah/grassland of North ...
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Haplogroup E-M2 (Y-DNA)
Haplogroup E-M2 (or E1b1a) is a human Y-chromosome DNA haplogroup. It is primarily distributed in sub-Saharan Africa. E-M2 is the predominant subclade in West-Central Africa, Southern Africa and the African Great Lakes, and occurs at moderate frequencies in North Africa and Middle East. E-M2 has several subclades, but many of these subhaplogroups are included in either E-L485 or E-U175. E-M2 is especially common in native Africans speaking Niger-Congo languages and was spread to Southern and Eastern Africa through the Bantu expansion. Origins The discovery of two SNPs (V38 and V100) by Trombetta et al. (2011) significantly redefined the E-V38 phylogenetic tree. This led the authors to suggest that E-V38 may have originated in East Africa. E-V38 joins the West African-affiliated E-M2 and the northern East African-affiliated E-M329 with an earlier common ancestor who, like E-P2, may have also originated in East Africa. The downstreams SNP E-M180 possibly originated on the moist so ...
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Haplogroup E-M2
Haplogroup E-M2 (or E1b1a) is a human Y-chromosome DNA haplogroup. It is primarily distributed in sub-Saharan Africa. E-M2 is the predominant subclade in West-Central Africa, Southern Africa and the African Great Lakes, and occurs at moderate frequencies in North Africa and Middle East. E-M2 has several subclades, but many of these subhaplogroups are included in either E-L485 or E-U175. E-M2 is especially common in native Africans speaking Niger-Congo languages and was spread to Southern and Eastern Africa through the Bantu expansion. Origins The discovery of two SNPs (V38 and V100) by Trombetta et al. (2011) significantly redefined the E-V38 phylogenetic tree. This led the authors to suggest that E-V38 may have originated in East Africa. E-V38 joins the West African-affiliated E-M2 and the northern East African-affiliated E-M329 with an earlier common ancestor who, like E-P2, may have also originated in East Africa. The downstreams SNP E-M180 possibly originated on the moist so ...
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Haplogroup E-M96 (Y-DNA)
Haplogroup E-M96 is a human Y-chromosome DNA haplogroup. It is one of the two main branches of the older and ancestral haplogroup DE, the other main branch being haplogroup D. The E-M96 clade is divided into two main subclades: the more common E-P147, and the less common E-M75. Origins Underhill (2001) proposed that haplogroup E may have arisen in East Africa. Some authors as Chandrasekar (2007), accept the earlier position of Hammer (1997) that Haplogroup E may have originated in West Asia, given that: * E is a clade of Haplogroup DE, with the other major clade, haplogroup D, being exclusively distributed in Asia. * DE is a clade within M168 with the other two major clades, C and F, considered to have already a Eurasian origin. However, several discoveries made since the Hammer articles are thought to make an Asian origin less likely: # Underhill and Kivisild (2007) demonstrated that C and F have a common ancestor meaning that DE has only one sibling which is non-African. ...
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Haplogroup E-M329
Haplogroup E-M329, also known as E1b1a2, is a human Y-chromosome DNA haplogroup. E-M329 is mostly found in East Africa. Origin Trombetta et al. (2011) suggested an origin in East Africa: The new topology here reported has important implications as to the origins of the haplogroup E-P2. Using the principle of the phylogeographic parsimony, the resolution of the E-M215 trifurcation in favor of a common ancestor of E-M2 and E-M329 strongly supports the hypothesis that haplogroup E-P2 originated in eastern Africa, as previously suggested, and that chromosomes E-M2, so frequently observed in sub-Saharan Africa, trace their descent to a common ancestor present in eastern Africa. Distribution E-M329 is mostly found in East Africa. E-M329 is frequent in Southwestern Ethiopia, especially among Omotic-speaking populations. Semino et al. (2004) found 2 cases of E-M329 in Ethiopian Oromo, out of 2400 individuals, including 78 Oromo. Cadenas et al. (2007) found one case of E-M329, o ...
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Haplogroup E-P2 (Y-DNA)
E-P2, also known as E1b1, is a human Y-chromosome DNA haplogroup. This paternal clade had an ancient presence in the Middle East, and is now primarily distributed in Africa where it's believed to have originated, with lower frequencies in the Middle East and Europe. Origin Trombetta et al. 2011, suggest an origin in eastern Africa: The new topology here reported has important implications as to the origins of the haplogroup E-P2. Using the principle of the phylogeographic parsimony, the resolution of the E-M215 trifurcation in favor of a common ancestor of E-M2 and E-M329 strongly supports the hypothesis that haplogroup E-P2 originated in eastern Africa, as previously suggested, and that chromosomes E-M2, so frequently observed in sub-Saharan Africa, trace their descent to a common ancestor present in eastern Africa. Distribution Natufian fossils that were analysed for ancient DNA were found to carry the paternal haplogroup E1b1(xE1b1a1,E1b1b1b1) (1/5; 20%). Table S6.1 – Y-c ...
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Haplogroup E-M75 (Y-DNA)
Haplogroup E-M75 is a human Y-chromosome DNA haplogroup. Along with haplogroup E-P147, it is one of the two main branches of the older haplogroup E-M96. Distribution Sorted frequency table of E-M75+ populations. Note that a "?" specifies that the sublineage of E-M75 was either untested for or unreported in the relevant study. Subclades Paragroup E-M75 Haplogroup E-M75(xM41,M54) has been found in 6% (1/18) of a sample of Dama from Namibia, 4% (1/26) of a sample of Ganda from Uganda, 3% (1/39) of a sample of Mandinka from Gambia/Senegal, and 2% (1/49) of a sample of Shona from Zimbabwe. E-M41 Haplogroup E-M41 has been found mainly in populations of the Great Lakes and Upper Nile regions of Central-East Africa, including 67% (6/9) of a sample of Alur from the DRC, 39% (7/18) of a sample of Hema from the DRC, 17% (15/88) of a sample from Ethiopia, 8% (2/26) of a sample of Ganda from Uganda, 5% (2/40) of a sample from Sudan, 4% (3/69) of a sample of Hutu from Rwanda, 3% (1/29) ...
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Haplogroup E-M33 (Y-DNA)
Haplogroup E-M132, formerly known as E-M33 (E1a), is a human Y-chromosome DNA haplogroup. Along with E-P177, it is one of the two main branches of the older E-P147 paternal clade. E-M132 is divided into two primary sub-branches, E-M44 and E-Z958, with many descendant subclades. Distribution E-M132 is found most often in West Africa, and today it is especially common in the region of Mali. One study has found haplogroup E-M132 Y-chromosomes in as much as 34% (15/44) of a sample of Malian men, including 2/44 E-M44 and 13/44 E-M33/M132(xE-M44).Peter A. Underhill, Peidong Shen, Alice A. Lin ''et al.'', "Y chromosome sequence variation and the history of human populations," ''Nature Genetics'', Volume 26, November 2000 In particular, the Dogon people of Mali have been found to carry haplogroup E-M132 with a frequency as high as 45.5% (25/55). This makes it perhaps the most common Y-DNA haplogroup in this population, though haplogroup E-P1 appears to be almost equally frequent am ...
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Human Y-chromosome DNA Haplogroup
In human genetics, a human Y-chromosome DNA haplogroup is a haplogroup defined by mutations in the non- recombining portions of DNA from the male-specific Y chromosome (called Y-DNA). Many people within a haplogroup share similar numbers of short tandem repeats (STRs) and types of mutations called single-nucleotide polymorphisms (SNPs). The human Y-chromosome accumulates roughly two mutations per generation. "one mutation in every 30 million base pairs" Y-DNA haplogroups represent major branches of the Y-chromosome phylogenetic tree that share hundreds or even thousands of mutations unique to each haplogroup. The Y-chromosomal most recent common ancestor (Y-MRCA, informally known as Y-chromosomal Adam) is the most recent common ancestor (MRCA) from whom all currently living humans are descended patrilineally. Y-chromosomal Adam is estimated to have lived roughly 236,000 years ago in Africa. By examining other bottlenecks most Eurasian men (men from populations outside ...
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Haplogroup E-M116
A haplotype is a group of alleles in an organism that are inherited together from a single parent, and a haplogroup ( haploid from the el, ἁπλοῦς, ''haploûs'', "onefold, simple" and en, group) is a group of similar haplotypes that share a common ancestor with a single-nucleotide polymorphism mutation. More specifically, a haplogroup is a combination of alleles at different chromosomal regions that are closely linked and that tend to be inherited together. As a haplogroup consists of similar haplotypes, it is usually possible to predict a haplogroup from haplotypes. Haplogroups pertain to a single line of descent. As such, membership of a haplogroup, by any individual, relies on a relatively small proportion of the genetic material possessed by that individual. Each haplogroup originates from, and remains part of, a preceding single haplogroup (or paragroup). As such, any related group of haplogroups may be precisely modelled as a nested hierarchy, in which each set (h ...
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Haplogroup
A haplotype is a group of alleles in an organism that are inherited together from a single parent, and a haplogroup (haploid from the el, ἁπλοῦς, ''haploûs'', "onefold, simple" and en, group) is a group of similar haplotypes that share a common ancestor with a single-nucleotide polymorphism mutation. More specifically, a haplogroup is a combination of alleles at different chromosomal regions that are closely linked and that tend to be inherited together. As a haplogroup consists of similar haplotypes, it is usually possible to predict a haplogroup from haplotypes. Haplogroups pertain to a single line of descent. As such, membership of a haplogroup, by any individual, relies on a relatively small proportion of the genetic material possessed by that individual. Each haplogroup originates from, and remains part of, a preceding single haplogroup (or paragroup). As such, any related group of haplogroups may be precisely modelled as a nested hierarchy, in which each set (ha ...
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Haplogroup E-M58 (Y-DNA)
A haplotype is a group of alleles in an organism that are inherited together from a single parent, and a haplogroup ( haploid from the el, ἁπλοῦς, ''haploûs'', "onefold, simple" and en, group) is a group of similar haplotypes that share a common ancestor with a single-nucleotide polymorphism mutation. More specifically, a haplogroup is a combination of alleles at different chromosomal regions that are closely linked and that tend to be inherited together. As a haplogroup consists of similar haplotypes, it is usually possible to predict a haplogroup from haplotypes. Haplogroups pertain to a single line of descent. As such, membership of a haplogroup, by any individual, relies on a relatively small proportion of the genetic material possessed by that individual. Each haplogroup originates from, and remains part of, a preceding single haplogroup (or paragroup). As such, any related group of haplogroups may be precisely modelled as a nested hierarchy, in which each set (h ...
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Haplogroup E-M54 (Y-DNA)
A haplotype is a group of alleles in an organism that are inherited together from a single parent, and a haplogroup (haploid from the el, ἁπλοῦς, ''haploûs'', "onefold, simple" and en, group) is a group of similar haplotypes that share a common ancestor with a single-nucleotide polymorphism mutation. More specifically, a haplogroup is a combination of alleles at different chromosomal regions that are closely linked and that tend to be inherited together. As a haplogroup consists of similar haplotypes, it is usually possible to predict a haplogroup from haplotypes. Haplogroups pertain to a single line of descent. As such, membership of a haplogroup, by any individual, relies on a relatively small proportion of the genetic material possessed by that individual. Each haplogroup originates from, and remains part of, a preceding single haplogroup (or paragroup). As such, any related group of haplogroups may be precisely modelled as a nested hierarchy, in which each set (ha ...
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