A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893378



Internal ID19184198
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:17338052..17372096hg38UCSC Ensembl
Outerchr21:17338052..17372096hg38UCSC Ensembl
Innerchr21:18710371..18744415hg19UCSC Ensembl
Outerchr21:18710371..18744415hg19UCSC Ensembl
Innerchr21:17632242..17666286hg18UCSC Ensembl
Outerchr21:17632242..17666286hg18UCSC Ensembl
Cytoband21q21.1
Allele length
AssemblyAllele length
hg3834045
hg1934045
hg1834045
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25779108, essv25784278
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893378
Frequency
Sample Size3017
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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