A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv554655



Internal ID16342064
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:54932058..55120957hg38UCSC Ensembl
Innerchr11:54699533..54888433hg19UCSC Ensembl
Innerchr11:54456109..54645009hg18UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg38188900
hg19188901
hg18188901
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1874n54
Supporting Variantsnssv774846
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv554655
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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