A curated catalogue of human genomic structural variation




Variant Details

Variant: esv274896



Internal ID347856
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:38207737..38208445hg38UCSC Ensembl
Outerchr3:38201009..38222109hg38UCSC Ensembl
Innerchr3:38249228..38249936hg19UCSC Ensembl
Outerchr3:38242500..38263600hg19UCSC Ensembl
Innerchr3:38224232..38224940hg18UCSC Ensembl
Outerchr3:38217504..38238604hg18UCSC Ensembl
Cytoband3p22.2
Allele length
AssemblyAllele length
hg3821101
hg1921101
hg1821101
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv2585471
Samples
Known GenesOXSR1
MethodSNP array
AnalysisIdentification of germline Changes in Copy Number (IgC2N)
PlatformAffymetrix SNP 6.0
Comments
ReferenceBanerjee_et_al_2011
Pubmed ID21479260
Accession Number(s)esv274896
Frequency
Sample Size1250
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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