A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv529003



Internal ID15456296
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:120338677..120484521hg38UCSC Ensembl
Innerchr11:120209386..120355230hg19UCSC Ensembl
Innerchr11:119714596..119860440hg18UCSC Ensembl
Innerchr11:119714596..119860440hg17UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg38145845
hg19145845
hg18145845
hg17145845
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv705710
Samples
Known GenesARHGEF12
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv529003
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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