A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv521672



Internal ID15448965
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:71951510..71960265hg38UCSC Ensembl
Innerchr9:74566426..74575181hg19UCSC Ensembl
Innerchr9:73756246..73765001hg18UCSC Ensembl
Innerchr9:71795980..71804735hg17UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg388756
hg198756
hg188756
hg178756
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv698290
Samples
Known GenesC9orf85
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv521672
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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