A curated catalogue of human genomic structural variation




Variant Details

Variant: essv2585998



Internal ID347577
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:36249758..36249830hg38UCSC Ensembl
Outerchr4:36249221..36253312hg38UCSC Ensembl
Innerchr4:36251380..36251452hg19UCSC Ensembl
Outerchr4:36250843..36254934hg19UCSC Ensembl
Innerchr4:35927775..35927847hg18UCSC Ensembl
Outerchr4:35927238..35931329hg18UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg384092
hg194092
hg184092
Variant TypeCNV loss
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv275504
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)essv2585998
Frequency
Sample Size1250
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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