A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17024215



Internal ID83880
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:67623193..67642000hg38UCSC Ensembl
chr9:46281666..46300511hg19UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg3818808
hg1918846
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6142722
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17024215
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.022843


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