A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16932162



Internal ID22166
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:31737689..31744966hg38UCSC Ensembl
chr3:31779181..31786458hg19UCSC Ensembl
Cytoband3p23
Allele length
AssemblyAllele length
hg387278
hg197278
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5436732
Supporting Variants
Samples
Known GenesOSBPL10
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16932162
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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