A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv699882



Internal ID15436534
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:76322330..76336749hg38UCSC Ensembl
Innerchr11:76033374..76047793hg19UCSC Ensembl
Innerchr11:75711022..75725441hg18UCSC Ensembl
Innerchr11:75711022..75725441hg17UCSC Ensembl
Cytoband11q13.5
Allele length
AssemblyAllele length
hg3814420
hg1914420
hg1814420
hg1714420
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv524020
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv699882
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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