A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893379



Internal ID19184199
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:17339103..17351832hg38UCSC Ensembl
Outerchr21:17338052..17351832hg38UCSC Ensembl
Innerchr21:18711422..18724151hg19UCSC Ensembl
Outerchr21:18710371..18724151hg19UCSC Ensembl
Innerchr21:17633293..17646022hg18UCSC Ensembl
Outerchr21:17632242..17646022hg18UCSC Ensembl
Cytoband21q21.1
Allele length
AssemblyAllele length
hg3813781
hg1913781
hg1813781
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25800667, essv25779556
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893379
Frequency
Sample Size3017
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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