A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv556593



Internal ID15997316
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:133043972..133725153hg38UCSC Ensembl
Innerchr11:132913867..133595048hg19UCSC Ensembl
Innerchr11:132419077..133100258hg18UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg38681182
hg19681182
hg18681182
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv785139
Samples
Known GenesOPCML
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv556593
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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