A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv554616



Internal ID15995339
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:54928232..55271002hg38UCSC Ensembl
Innerchr11:54695707..55038478hg19UCSC Ensembl
Innerchr11:54452283..54795054hg18UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg38342771
hg19342772
hg18342772
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1865n54
Supporting Variantsnssv774765
Samples
Known GenesTRIM48
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv554616
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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