A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893290



Internal ID18837424
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:14153723..14357847hg38UCSC Ensembl
Outerchr20:14153723..14357847hg38UCSC Ensembl
Innerchr20:14134369..14338493hg19UCSC Ensembl
Outerchr20:14134369..14338493hg19UCSC Ensembl
Innerchr20:14082369..14286493hg18UCSC Ensembl
Outerchr20:14082369..14286493hg18UCSC Ensembl
Cytoband20p12.1
Allele length
AssemblyAllele length
hg38204125
hg19204125
hg18204125
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25789445
Samples
Known GenesFLRT3, MACROD2
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893290
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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