A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2173n54



Internal ID22770068
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:107370321..107372701hg38UCSC Ensembl
chr11:107241047..107243427hg19UCSC Ensembl
chr11:106746257..106748637hg18UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg382381
hg192381
hg182381
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv556365, nsv556373, nsv556363, nsv556371, nsv556370, nsv556374, nsv556361, nsv556364, nsv556369, nsv556360, nsv556366, nsv556367, nsv556368, nsv556362
Samples
Known GenesCWF19L2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv2173n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss19
Observed Complex0
Frequencyn/a


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