A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv556352



Internal ID16343761
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:107369763..107370809hg38UCSC Ensembl
Innerchr11:107240489..107241535hg19UCSC Ensembl
Innerchr11:106745699..106746745hg18UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg381047
hg191047
hg181047
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2170n54
Supporting Variantsnssv784177
Samples
Known GenesCWF19L2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv556352
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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