A curated catalogue of human genomic structural variation




Variant Details

Variant: essv2586156



Internal ID1049
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:41202251..41213598hg38UCSC Ensembl
Outerchr3:41202225..41213720hg38UCSC Ensembl
Innerchr3:41243742..41255089hg19UCSC Ensembl
Outerchr3:41243716..41255211hg19UCSC Ensembl
Innerchr3:41218746..41230093hg18UCSC Ensembl
Outerchr3:41218720..41230215hg18UCSC Ensembl
Cytoband3p22.1
Allele length
AssemblyAllele length
hg3811496
hg1911496
hg1811496
Variant TypeCNV loss
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv274874
Supporting Variants
Samples
Known GenesCTNNB1
MethodSNP array
AnalysisIdentification of germline Changes in Copy Number (IgC2N)
PlatformAffymetrix SNP 6.0
Comments
ReferenceBanerjee_et_al_2011
Pubmed ID21479260
Accession Number(s)essv2586156
Frequency
Sample Size1250
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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