A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv668901



Internal ID15058867
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:46092442..46172742hg38UCSC Ensembl
Innerchr17:44169808..44250108hg19UCSC Ensembl
Innerchr17:41525626..41605885hg18UCSC Ensembl
Innerchr17:41525626..41605885hg17UCSC Ensembl
Cytoband17q21.31
Allele length
AssemblyAllele length
hg3880301
hg1980301
hg1880260
hg1780260
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516807
Supporting Variants
Samples
Known GenesKANSL1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv668901
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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