A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv665191



Internal ID15055157
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:112604798..112826971hg38UCSC Ensembl
Innerchr9:115367078..115589251hg19UCSC Ensembl
Innerchr9:114406899..114629072hg18UCSC Ensembl
Innerchr9:112446633..112668806hg17UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg38222174
hg19222174
hg18222174
hg17222174
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv515899
Supporting Variants
Samples
Known GenesINIP, KIAA1958, SNX30
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv665191
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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