Variation class
mobile element insertion(SO:0001837)
Allele type(s)
HERV insertion(SO:0002187)
Source
dbVar - NCBI database of human genomic structural variation
Study
nstd152 - Chaisson 2018 "This is an integrated callset from three individuals (HG00514, HG00733, and NA19240) sequenced using Illumina, Illumina 3.5 kbp jumping libraries, Illumina 6kbp jumping libraries, PacBio, BioNano Genomics, 10x, Hi-C, and Strand-seq."
Alias
9__86588253___86588254______GRCh38_herv_insertion
Location
Chromosome 9:89203168 (forward strand) | View in location tab
About this structural variant
This structural variant is associated with 1 phenotype and is supported by 1 piece of evidence.
