A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17023467



Internal ID83364
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:32743956..32744025hg38UCSC Ensembl
chr9:32743954..32744023hg19UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg3870
hg1970
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5474460
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17023467
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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