A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv692817



Internal ID15082783
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:112596769..112831590hg38UCSC Ensembl
Innerchr9:115359049..115593870hg19UCSC Ensembl
Innerchr9:114398870..114633691hg18UCSC Ensembl
Innerchr9:112438604..112673425hg17UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg38234822
hg19234822
hg18234822
hg17234822
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)nssv692817
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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