A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv614655



Internal ID16402064
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:73583536..73631371hg38UCSC Ensembl
Innerchr9:76198452..76246287hg19UCSC Ensembl
Innerchr9:75388272..75436107hg18UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg3847836
hg1947836
hg1847836
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1137321
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv614655
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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