A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv553293



Internal ID16340702
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:5739717..5740331hg38UCSC Ensembl
Innerchr11:5760947..5761561hg19UCSC Ensembl
Innerchr11:5717523..5718137hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg38615
hg19615
hg18615
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1613n54
Supporting Variantsnssv765886
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv553293
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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