A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893998



Internal ID19184852
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:101501065..101562626hg38UCSC Ensembl
Outerchr4:101501065..101562626hg38UCSC Ensembl
Innerchr4:102422222..102483783hg19UCSC Ensembl
Outerchr4:102422222..102483783hg19UCSC Ensembl
Innerchr4:102641245..102702806hg18UCSC Ensembl
Outerchr4:102641245..102702806hg18UCSC Ensembl
Cytoband4q24
Allele length
AssemblyAllele length
hg3861562
hg1961562
hg1861562
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25784078, essv25800985
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893998
Frequency
Sample Size3017
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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