A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv556282



Internal ID16343691
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:107347678..107372480hg38UCSC Ensembl
Innerchr11:107218404..107243206hg19UCSC Ensembl
Innerchr11:106723614..106748416hg18UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg3824803
hg1924803
hg1824803
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv783729
Samples
Known GenesCWF19L2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv556282
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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