A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv668624



Internal ID15405276
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:46587..272191hg38UCSC Ensembl
Innerchr9:46587..272191hg19UCSC Ensembl
Innerchr9:36587..262191hg18UCSC Ensembl
Innerchr9:36587..262191hg17UCSC Ensembl
Cytoband9p24.3
Allele length
AssemblyAllele length
hg38225605
hg19225605
hg18225605
hg17225605
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)nssv668624
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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