A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv690094



Internal ID15426746
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:12574460..12584561hg38UCSC Ensembl
Innerchr11:12596007..12606108hg19UCSC Ensembl
Innerchr11:12552583..12562684hg18UCSC Ensembl
Innerchr11:12552583..12562684hg17UCSC Ensembl
Cytoband11p15.3
Allele length
AssemblyAllele length
hg3810102
hg1910102
hg1810102
hg1710102
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv520324
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv690094
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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