A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv660858



Internal ID15050824
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:33155427..33270750hg38UCSC Ensembl
Innerchr9:33155425..33270748hg19UCSC Ensembl
Innerchr9:33145425..33260748hg18UCSC Ensembl
Innerchr9:33145425..33260748hg17UCSC Ensembl
Cytoband9p13.3
Allele length
AssemblyAllele length
hg38115324
hg19115324
hg18115324
hg17115324
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv519369
Supporting Variants
Samples
Known GenesB4GALT1, BAG1, CHMP5, LOC101929639, SPINK4
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv660858
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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