A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv692287



Internal ID15428939
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:46587..281976hg38UCSC Ensembl
Innerchr9:46587..281976hg19UCSC Ensembl
Innerchr9:36587..271976hg18UCSC Ensembl
Innerchr9:36587..271976hg17UCSC Ensembl
Cytoband9p24.3
Allele length
AssemblyAllele length
hg38235390
hg19235390
hg18235390
hg17235390
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv515505
Supporting Variants
Samples
Known GenesC9orf66, CBWD1, DOCK8, FOXD4
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv692287
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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