A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16940762



Internal ID27876
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:145582910..145582944hg38UCSC Ensembl
chr3:145300697..145300731hg19UCSC Ensembl
Cytoband3q24
Allele length
AssemblyAllele length
hg38321
hg19321
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5553905
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16940762
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.002185


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