A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv523356



Internal ID15103963
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:33755788..33775862hg38UCSC Ensembl
Innerchr11:33777334..33797408hg19UCSC Ensembl
Innerchr11:33733910..33753984hg18UCSC Ensembl
Innerchr11:33733910..33753984hg17UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg3820075
hg1920075
hg1820075
hg1720075
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv699105
Samples
Known GenesFBXO3
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv523356
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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