A curated catalogue of human genomic structural variation




Variant Details

Variant: esv274965



Internal ID347812
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:4798891..4799343hg38UCSC Ensembl
Outerchr20:4795875..4799774hg38UCSC Ensembl
Innerchr20:4779537..4779989hg19UCSC Ensembl
Outerchr20:4776521..4780420hg19UCSC Ensembl
Innerchr20:4727537..4727989hg18UCSC Ensembl
Outerchr20:4724521..4728420hg18UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg383900
hg193900
hg183900
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv2585650
Samples
Known GenesRASSF2
MethodSNP array
AnalysisIdentification of germline Changes in Copy Number (IgC2N)
PlatformAffymetrix SNP 6.0
Comments
ReferenceBanerjee_et_al_2011
Pubmed ID21479260
Accession Number(s)esv274965
Frequency
Sample Size1250
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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