A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893319



Internal ID19184139
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:17204995..17214420hg38UCSC Ensembl
Outerchr20:17204995..17214420hg38UCSC Ensembl
Innerchr20:17185640..17195065hg19UCSC Ensembl
Outerchr20:17185640..17195065hg19UCSC Ensembl
Innerchr20:17133640..17143065hg18UCSC Ensembl
Outerchr20:17133640..17143065hg18UCSC Ensembl
Cytoband20p12.1
Allele length
AssemblyAllele length
hg389426
hg199426
hg189426
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25786196
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893319
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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