A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv520466



Internal ID15447759
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:86633635..86635898hg38UCSC Ensembl
Innerchr11:86344677..86346940hg19UCSC Ensembl
Innerchr11:86022325..86024588hg18UCSC Ensembl
Innerchr11:86022325..86024588hg17UCSC Ensembl
Cytoband11q14.2
Allele length
AssemblyAllele length
hg382264
hg192264
hg182264
hg172264
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv697437
Samples
Known GenesME3
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv520466
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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