A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv662594



Internal ID15399246
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:46587..426215hg38UCSC Ensembl
Innerchr9:46587..426215hg19UCSC Ensembl
Innerchr9:36587..416215hg18UCSC Ensembl
Innerchr9:36587..416215hg17UCSC Ensembl
Cytoband9p24.3
Allele length
AssemblyAllele length
hg38379629
hg19379629
hg18379629
hg17379629
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)nssv662594
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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