A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv613616



Internal ID16401025
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:12922331..13018097hg38UCSC Ensembl
Innerchr9:12922330..13018096hg19UCSC Ensembl
Innerchr9:12912330..13008096hg18UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg3895767
hg1995767
hg1895767
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1128718
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv613616
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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