A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2163n54



Internal ID22770058
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:107368380..107370321hg38UCSC Ensembl
chr11:107239106..107241047hg19UCSC Ensembl
chr11:106744316..106746257hg18UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg381942
hg191942
hg181942
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv556291, nsv556309, nsv556323, nsv556290, nsv556322, nsv556310
Samples
Known GenesCWF19L2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv2163n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss23
Observed Complex0
Frequencyn/a


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