A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv556369



Internal ID16343778
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:107370601..107372252hg38UCSC Ensembl
Innerchr11:107241327..107242978hg19UCSC Ensembl
Innerchr11:106746537..106748188hg18UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg381652
hg191652
hg181652
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2173n54
Supporting Variantsnssv784197, nssv784196
Samples
Known GenesCWF19L2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv556369
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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