A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv766937



Internal ID16060893
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:7114550..7124807hg38UCSC Ensembl
Innerchr11:7135781..7146038hg19UCSC Ensembl
Innerchr11:7092357..7102614hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3810258
hg1910258
hg1810258
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv553404
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv766937
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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