A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17686973



Internal ID110639
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:37885681..37885759hg38UCSC Ensembl
chr13:38459818..38459896hg19UCSC Ensembl
Cytoband13q13.3
Allele length
AssemblyAllele length
hg3879
hg1979
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6143677
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17686973
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.12972


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