A curated catalogue of human genomic structural variation




Variant Details

Variant: essv2586047



Internal ID347626
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 OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv274990
Supporting Variants
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)essv2586047
Frequency
Sample Size1250
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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