A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3894025



Internal ID19184879
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:124942819..125138066hg38UCSC Ensembl
Outerchr4:124910059..125145549hg38UCSC Ensembl
Innerchr4:125863974..126059221hg19UCSC Ensembl
Outerchr4:125831214..126066704hg19UCSC Ensembl
Innerchr4:126083424..126278671hg18UCSC Ensembl
Outerchr4:126050664..126286154hg18UCSC Ensembl
Cytoband4q28.1
Allele length
AssemblyAllele length
hg38235491
hg19235491
hg18235491
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25788088, essv25788126, essv25788143
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3894025
Frequency
Sample Size3017
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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