A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17021535



Internal ID82003
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:35052000..35112000hg38UCSC Ensembl
chr9:35051997..35111997hg19UCSC Ensembl
Cytoband9p13.3
Allele length
AssemblyAllele length
hg3860001
hg1960001
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6141848
Supporting Variants
Samples
Known GenesFAM214B, FANCG, PIGO, STOML2, VCP
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17021535
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000471


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