A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv555836



Internal ID15996559
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:90309371..90364091hg38UCSC Ensembl
Innerchr11:90042539..90097259hg19UCSC Ensembl
Innerchr11:89682187..89736907hg18UCSC Ensembl
Cytoband11q14.3
Allele length
AssemblyAllele length
hg3854721
hg1954721
hg1854721
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv780548
Samples
Known GenesDISC1FP1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv555836
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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