A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv700388



Internal ID15437040
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:20532143..20544830hg38UCSC Ensembl
Innerchr11:20553689..20566376hg19UCSC Ensembl
Innerchr11:20510265..20522952hg18UCSC Ensembl
Innerchr11:20510265..20522952hg17UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg3812688
hg1912688
hg1812688
hg1712688
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv524455
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv700388
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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