A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv556351



Internal ID16343760
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:107369524..107372262hg38UCSC Ensembl
Innerchr11:107240250..107242988hg19UCSC Ensembl
Innerchr11:106745460..106748198hg18UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg382739
hg192739
hg182739
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2169n54
Supporting Variantsnssv784175, nssv784176
Samples
Known GenesCWF19L2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv556351
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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