A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2169n54



Internal ID22770064
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:107368911..107372701hg38UCSC Ensembl
chr11:107239637..107243427hg19UCSC Ensembl
chr11:106744847..106748637hg18UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg383791
hg193791
hg183791
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv556348, nsv556340, nsv556333, nsv556341, nsv556342, nsv556356, nsv556334, nsv556349, nsv556346, nsv556351, nsv556336, nsv556355, nsv556347, nsv556331, nsv556332
Samples
Known GenesCWF19L2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv2169n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss19
Observed Complex0
Frequencyn/a


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