A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv556586



Internal ID15997309
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:132057809..132060294hg38UCSC Ensembl
Innerchr11:131927703..131930188hg19UCSC Ensembl
Innerchr11:131432913..131435398hg18UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg382486
hg192486
hg182486
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2202n54
Supporting Variantsnssv785130, nssv785131
Samples
Known GenesNTM
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv556586
Frequency
Sample Size17421
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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