A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17021362



Internal ID81882
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:31009193..31029393hg38UCSC Ensembl
chr9:31009191..31029391hg19UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg3820201
hg1920201
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5484677
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17021362
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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