A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17692032



Internal ID115698
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:65220192..65318388hg38UCSC Ensembl
chr13:65794324..65892520hg19UCSC Ensembl
Cytoband13q21.32
Allele length
AssemblyAllele length
hg3898197
hg1998197
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5504880
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17692032
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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