A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893384



Internal ID19184204
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:18685601..18706106hg38UCSC Ensembl
Outerchr21:18682124..18706106hg38UCSC Ensembl
Innerchr21:20057919..20078424hg19UCSC Ensembl
Outerchr21:20054442..20078424hg19UCSC Ensembl
Innerchr21:18979790..19000295hg18UCSC Ensembl
Outerchr21:18976313..19000295hg18UCSC Ensembl
Cytoband21q21.1
Allele length
AssemblyAllele length
hg3823983
hg1923983
hg1823983
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25790491, essv25790509
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893384
Frequency
Sample Size3017
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer