A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16931813



Internal ID21940
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:37562949..37562969hg38UCSC Ensembl
chr3:37604440..37604460hg19UCSC Ensembl
Cytoband3p22.2
Allele length
AssemblyAllele length
hg38310
hg19310
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5540290
Supporting Variants
Samples
Known GenesITGA9
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16931813
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.107868


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