A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16936289



Internal ID24921
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:81971297..81974775hg38UCSC Ensembl
chr3:82020448..82023926hg19UCSC Ensembl
Cytoband3p12.2
Allele length
AssemblyAllele length
hg383479
hg193479
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5435880
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16936289
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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