A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17616626



Internal ID21808673
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:38345031..38345031hg38UCSC Ensembl
chr13:38919168..38919168hg19UCSC Ensembl
Cytoband13q13.3
Allele length
AssemblyAllele length
hg382544
hg192544
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6089366
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17616626
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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