A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17020217



Internal ID81111
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:27640574..27641584hg38UCSC Ensembl
chr9:27640572..27641582hg19UCSC Ensembl
Cytoband9p21.2
Allele length
AssemblyAllele length
hg381011
hg191011
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5491459
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17020217
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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