A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17022484



Internal ID82671
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:21227652..21239414hg38UCSC Ensembl
chr9:21227651..21239413hg19UCSC Ensembl
Cytoband9p21.3
Allele length
AssemblyAllele length
hg3811763
hg1911763
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5486038
Supporting Variants
Samples
Known GenesIFNA14, IFNA17
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17022484
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000468


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