A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25792155



Internal ID19170004
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:13859439..13945546hg38UCSC Ensembl
Innerchr21:15231760..15317867hg19UCSC Ensembl
Innerchr21:14153631..14239738hg18UCSC Ensembl
Cytoband21q11.2
Allele length
AssemblyAllele length
hg3886108
hg1986108
hg1886108
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=21
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25792155
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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