A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893275



Internal ID19184095
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:5630091..5720835hg38UCSC Ensembl
Outerchr20:5630091..5720835hg38UCSC Ensembl
Innerchr20:5610737..5701481hg19UCSC Ensembl
Outerchr20:5610737..5701481hg19UCSC Ensembl
Innerchr20:5558737..5649481hg18UCSC Ensembl
Outerchr20:5558737..5649481hg18UCSC Ensembl
Cytoband20p12.3
Allele length
AssemblyAllele length
hg3890745
hg1990745
hg1890745
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25792650
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893275
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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