A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893363



Internal ID19184183
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:13859439..13945546hg38UCSC Ensembl
Outerchr21:13849437..13977705hg38UCSC Ensembl
Innerchr21:15231760..15317867hg19UCSC Ensembl
Outerchr21:15221758..15350026hg19UCSC Ensembl
Innerchr21:14153631..14239738hg18UCSC Ensembl
Outerchr21:14143629..14271897hg18UCSC Ensembl
Cytoband21q11.2
Allele length
AssemblyAllele length
hg38128269
hg19128269
hg18128269
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25791521, essv25792121, essv25791373, essv25792038, essv25792155, essv25790438, essv25792465
Samples
Known GenesANKRD20A11P
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893363
Frequency
Sample Size3017
Observed Gain7
Observed Loss0
Observed Complex0
Frequencyn/a


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