A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv696291



Internal ID15432943
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:114801197..114811651hg38UCSC Ensembl
Innerchr11:114671919..114682373hg19UCSC Ensembl
Innerchr11:114177129..114187583hg18UCSC Ensembl
Innerchr11:114177129..114187583hg17UCSC Ensembl
Cytoband11q23.2
Allele length
AssemblyAllele length
hg3810455
hg1910455
hg1810455
hg1710455
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv518838
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv696291
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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