A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893376



Internal ID19184196
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:17098391..17319089hg38UCSC Ensembl
Outerchr21:17098391..17319089hg38UCSC Ensembl
Innerchr21:18470709..18691408hg19UCSC Ensembl
Outerchr21:18470709..18691408hg19UCSC Ensembl
Innerchr21:17392580..17613279hg18UCSC Ensembl
Outerchr21:17392580..17613279hg18UCSC Ensembl
Cytoband21q21.1
Allele length
AssemblyAllele length
hg38220699
hg19220700
hg18220700
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25784714
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893376
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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