A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv699096



Internal ID15089062
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:5287498..5288465hg38UCSC Ensembl
Innerchr11:5308728..5309695hg19UCSC Ensembl
Innerchr11:5265304..5266271hg18UCSC Ensembl
Innerchr11:5265304..5266271hg17UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg38968
hg19968
hg18968
hg17968
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv523347
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv699096
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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