A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893274



Internal ID19184094
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:5398218..5496963hg38UCSC Ensembl
Outerchr20:5396865..5497596hg38UCSC Ensembl
Innerchr20:5378864..5477609hg19UCSC Ensembl
Outerchr20:5377511..5478242hg19UCSC Ensembl
Innerchr20:5326864..5425609hg18UCSC Ensembl
Outerchr20:5325511..5426242hg18UCSC Ensembl
Cytoband20p12.3
Allele length
AssemblyAllele length
hg38100732
hg19100732
hg18100732
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25792676, essv25789129
Samples
Known GenesLINC00658, LOC643406
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893274
Frequency
Sample Size3017
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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