A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv554911



Internal ID15995634
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:55606497..55626700hg38UCSC Ensembl
Innerchr11:55373973..55394176hg19UCSC Ensembl
Innerchr11:55130549..55150752hg18UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg3820204
hg1920204
hg1820204
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1918n54
Supporting Variantsnssv776522
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv554911
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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