A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16932145



Internal ID22155
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:31455468..31455564hg38UCSC Ensembl
chr3:31496960..31497056hg19UCSC Ensembl
Cytoband3p23
Allele length
AssemblyAllele length
hg3897
hg1997
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5453094
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16932145
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.012332


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