A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv614136



Internal ID16401545
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:31977625..32087234hg38UCSC Ensembl
Innerchr9:31977623..32087232hg19UCSC Ensembl
Innerchr9:31967623..32077232hg18UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg38109610
hg19109610
hg18109610
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12657n54
Supporting Variantsnssv1132824
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv614136
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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