A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv556585



Internal ID15997308
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:132057809..132059941hg38UCSC Ensembl
Innerchr11:131927703..131929835hg19UCSC Ensembl
Innerchr11:131432913..131435045hg18UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg382133
hg192133
hg182133
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2202n54
Supporting Variantsnssv785129
Samples
Known GenesNTM
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv556585
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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