A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893325



Internal ID19184145
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:25805665..25970656hg38UCSC Ensembl
Outerchr20:25805665..25971674hg38UCSC Ensembl
Innerchr20:25786301..25951292hg19UCSC Ensembl
Outerchr20:25786301..25952310hg19UCSC Ensembl
Innerchr20:25734301..25899292hg18UCSC Ensembl
Outerchr20:25734301..25900310hg18UCSC Ensembl
Cytoband20p11.1
Allele length
AssemblyAllele length
hg38166010
hg19166010
hg18166010
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25785829, essv25790639
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893325
Frequency
Sample Size3017
Observed Gain1
Observed Loss1
Observed Complex0
Frequencyn/a


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