A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv613931



Internal ID16401340
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:26259928..26276775hg38UCSC Ensembl
Innerchr9:26259926..26276773hg19UCSC Ensembl
Innerchr9:26249926..26266773hg18UCSC Ensembl
Cytoband9p21.2
Allele length
AssemblyAllele length
hg3816848
hg1916848
hg1816848
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12616n54
Supporting Variantsnssv1132060
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv613931
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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