In human genetics, Human Y-chromosome DNA haplogroups are haplogroups defined by differences in the DNA of the Y chromosome (called Y-DNA).
Y-DNA haplogroups are lettered A through R, and are further subdivided using numbers and lower case letters. Y chromosome haplogroup designations are established by the Y Chromosome Consortium .
Y-chromosomal Adam is the name given by researchers to the male who is the most recent common patrilineal (male-lineage) ancestor of all living humans. Note that while patrilinear separation of living humans dates to about 80,000 years ago (80 kya), the matrilinear tree preserves considerably older lineages, separation of living humans dating to ca. 150 kya.
Major Y-chromosome haplogroups include:
Haplogroups A and B are only found in sub-Saharan Africa (and in populations extracted from there in modern times, primarily via Atlantic slave trade). The first to branch off was A, with defining mutation M91. All other haplogroups are summarized as BR (also referred to as YxA).
The defining mutation separating CR (all haplogroups excepting A and B) are M168 and M294. These mutations predate the "Out of Africa" migration. The defining mutations of DE probably occurred in North Eastern Africa some 50 kya.
The bulk of haplogroup R is represented in lineages R1a and R1b. R1a likely originated in the Eurasian Steppes, and is associated with the Kurgan culture and Proto-Indo-European expansion. It is primarily found in Central and Western Asia, India, and the Slavic peoples of Eastern Europe. R1b originated prior to or during the last glaciation, when it was concentrated in refugia in southern Europe. It is most commonly found in European populations, especially in the west of Ireland.
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