A curated catalogue of human genomic structural variation




Variant Details

Variant: esv274990



Internal ID347896
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:36013359..36013896hg38UCSC Ensembl
Outerchr4:36012790..36015896hg38UCSC Ensembl
Innerchr4:36014981..36015518hg19UCSC Ensembl
Outerchr4:36014412..36017518hg19UCSC Ensembl
Innerchr4:35691376..35691913hg18UCSC Ensembl
Outerchr4:35690807..35693913hg18UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg383107
hg193107
hg183107
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv2586047
Samples
Known Genes
MethodSNP array
AnalysisIdentification of germline Changes in Copy Number (IgC2N)
PlatformAffymetrix SNP 6.0
Comments
ReferenceBanerjee_et_al_2011
Pubmed ID21479260
Accession Number(s)esv274990
Frequency
Sample Size1250
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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