A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv525837



Internal ID15106444
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:128969261..128972978hg38UCSC Ensembl
Innerchr11:128839156..128842873hg19UCSC Ensembl
Innerchr11:128344366..128348083hg18UCSC Ensembl
Innerchr11:128344366..128348083hg17UCSC Ensembl
Cytoband11q24.3
Allele length
AssemblyAllele length
hg383718
hg193718
hg183718
hg173718
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv702029
Samples
Known GenesARHGAP32
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv525837
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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