A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv695227



Internal ID15431879
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:57961521..57983529hg38UCSC Ensembl
Innerchr11:57728993..57751001hg19UCSC Ensembl
Innerchr11:57485569..57507577hg18UCSC Ensembl
Innerchr11:57485569..57507577hg17UCSC Ensembl
Cytoband11q12.1
Allele length
AssemblyAllele length
hg3822009
hg1922009
hg1822009
hg1722009
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517822
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv695227
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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