A curated catalogue of human genomic structural variation




Variant Details

Variant: esv274874



Internal ID1812374
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:41243742..41255089hg19UCSC Ensembl
Outerchr3:41243716..41255211hg19UCSC Ensembl
Innerchr3:41218746..41230093hg18UCSC Ensembl
Outerchr3:41218720..41230215hg18UCSC Ensembl
Cytoband3p22.1
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
Variant TypeCNV Loss
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Merged StatusS
Merged Variants
Supporting Variantsessv2586156
Samples
Known GenesCTNNB1
Method
AnalysisSV_analysis_a1
PlatformAffymetrix SNP 6.0
Comments
ReferenceBanerjee et al 2011
Pubmed ID21479260
Accession Number(s)esv274874
Frequency
Sample Size1250
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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