A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv554611



Internal ID16342020
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:54928232..55068990hg38UCSC Ensembl
Innerchr11:54695707..54836466hg19UCSC Ensembl
Innerchr11:54452283..54593042hg18UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg38140759
hg19140760
hg18140760
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv774758
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv554611
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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