A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv613927



Internal ID16401336
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:26153795..26284319hg38UCSC Ensembl
Innerchr9:26153793..26284317hg19UCSC Ensembl
Innerchr9:26143793..26274317hg18UCSC Ensembl
Cytoband9p21.2
Allele length
AssemblyAllele length
hg38130525
hg19130525
hg18130525
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1132056
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv613927
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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