DNA Marker Index information for Chromosome: Y Marker: FGC34960.1
Names and Aliases for this DNA Marker: FGC34960.1, FGC34960, Y20264.1, Y20264.
Chromosome Position in hg38 Human Genome assembly1: 21429544.
Chromosome Position in hg19 assembly2: 23591430 .
Ancestral marker allele value: A.
Derived, alternative, or mutated marker allele value: del.


DNA Marker Index data for Marker: FGC34960.1 on Chromosome: Y
Marker Name(s) Notes Identification Ancestral7 Derived8 Chromosome Position (hg38)1 Position (hg19)2
R-FGC34960 
FGC34960.1 FGC34960 Y20264.1 Y20264
 Found in haplogroup R1b under U106 and FGC34929 on YFull and FTDNA trees. Deletion of one base pair in a series of repeating alleles, 5A->4A. Also enumerated as hg38:21429539-GAAAAA-GAAAA and hg38:21429543-AA-A and hg38:21429539-GAAAAAT-GAAAATG. FTDNA uses the .1 suffix for different allele expressions which are equivalent. Example is GMP03755.
DNA lineage FGC34960.1 is estimated to have originated in about the year 90 ce based on its position in the phylogenetic tree.
Phylogenetic Parent: FGC34929 
View Ancestry 
Phylogenetic Children: FT75059  S27466 		 Full Genomes Corp 2015
A
del
Y
 21429544
23591430

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