Human (GRCh38.p14)
Variation class

short tandem repeat variation(SO:0002096)

Allele type(s)

short tandem repeat variation(SO:0002096)

Source

DGVa - Database of Genomic Variants Archive

Study

nstd128 - Mallick 2016 "We report high quality genomes from 300 individuals from 142 diverse populations. As part of this study, we generated a comprehensive catalog of short tandem repeat (STR) genotypes. We used this call set to characterize allele frequency spectra, analyze sequence determinants of STR variation, and to identify common loss of function alleles."

Alias

chrY_6677_alt_8_M

Location

Chromosome Y:56887112-56887141 (forward strand) | View in location tab

About this structural variant

This structural variant is supported by 9 pieces of evidence.