A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv520183



Internal ID15447476
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:16209183..16211322hg38UCSC Ensembl
Innerchr9:16209181..16211320hg19UCSC Ensembl
Innerchr9:16199181..16201320hg18UCSC Ensembl
Innerchr9:16199181..16201320hg17UCSC Ensembl
Cytoband9p22.3
Allele length
AssemblyAllele length
hg382140
hg192140
hg182140
hg172140
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv661461, nssv693124
Samples
Known GenesC9orf92
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv520183
Frequency
Sample Size2026
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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