A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16930502



Internal ID21081
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:16694317..16694358hg38UCSC Ensembl
chr3:16735824..16735865hg19UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg38322
hg19322
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5545778
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16930502
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.010771


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