A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1129322



Internal ID15982508
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:16963865..17070635hg38UCSC Ensembl
Innerchr9:16963863..17070633hg19UCSC Ensembl
Innerchr9:16953863..17060633hg18UCSC Ensembl
Cytoband9p22.2
Allele length
AssemblyAllele length
hg38106771
hg19106771
hg18106771
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv613692
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1129322
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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