A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv613744



Internal ID16401153
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:20286084..20292195hg38UCSC Ensembl
Innerchr9:20286082..20292193hg19UCSC Ensembl
Innerchr9:20276082..20282193hg18UCSC Ensembl
Cytoband9p21.3
Allele length
AssemblyAllele length
hg386112
hg196112
hg186112
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1130794
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv613744
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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