A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv553993



Internal ID16341402
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:33030935..33033097hg38UCSC Ensembl
Innerchr11:33052481..33054643hg19UCSC Ensembl
Innerchr11:33009057..33011219hg18UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg382163
hg192163
hg182163
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv771052
Samples
Known GenesDEPDC7
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv553993
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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