A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv554613



Internal ID16342022
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:54928232..55203117hg38UCSC Ensembl
Innerchr11:54695707..54970593hg19UCSC Ensembl
Innerchr11:54452283..54727169hg18UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg38274886
hg19274887
hg18274887
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1863n54
Supporting Variantsnssv774762, nssv774761, nssv774760
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv554613
Frequency
Sample Size17421
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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