A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25792038



Internal ID19165233
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:13849437..13964098hg38UCSC Ensembl
Innerchr21:15221758..15336419hg19UCSC Ensembl
Innerchr21:14143629..14258290hg18UCSC Ensembl
Cytoband21q11.2
Allele length
AssemblyAllele length
hg38114662
hg19114662
hg18114662
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3893363
Supporting Variants
Samples
Known GenesANKRD20A11P
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=23
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25792038
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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