A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv613739



Internal ID16401148
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:20075293..20096392hg38UCSC Ensembl
Innerchr9:20075291..20096390hg19UCSC Ensembl
Innerchr9:20065291..20086390hg18UCSC Ensembl
Cytoband9p21.3
Allele length
AssemblyAllele length
hg3821100
hg1921100
hg1821100
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1130789
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv613739
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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