A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv555600



Internal ID16343009
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:82554105..82716522hg38UCSC Ensembl
Innerchr11:82265147..82427564hg19UCSC Ensembl
Innerchr11:81942795..82105212hg18UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg38162418
hg19162418
hg18162418
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv779842
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv555600
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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