A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16936214



Internal ID24867
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:81014465..81015483hg38UCSC Ensembl
chr3:81063616..81064634hg19UCSC Ensembl
Cytoband3p12.2
Allele length
AssemblyAllele length
hg381019
hg191019
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6140137
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16936214
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.001405


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