A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv553354



Internal ID16340763
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:6094808..6097153hg38UCSC Ensembl
Innerchr11:6116038..6118383hg19UCSC Ensembl
Innerchr11:6072614..6074959hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg382346
hg192346
hg182346
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv766307
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv553354
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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