A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv517822



Internal ID15445115
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 State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv695227
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv517822
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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