A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893265



Internal ID19184085
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:611175..641181hg38UCSC Ensembl
Outerchr20:611175..641181hg38UCSC Ensembl
Innerchr20:591819..621825hg19UCSC Ensembl
Outerchr20:591819..621825hg19UCSC Ensembl
Innerchr20:539819..569825hg18UCSC Ensembl
Outerchr20:539819..569825hg18UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg3830007
hg1930007
hg1830007
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25796687
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893265
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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