A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17024220



Internal ID83884
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:67689387..67695387hg38UCSC Ensembl
chr9:46355223..46360919hg19UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg386001
hg195697
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6142160
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17024220
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.032967


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