A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25791467



Internal ID18829147
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:23630722..23961231hg38UCSC Ensembl
Innerchr20:23611359..23941868hg19UCSC Ensembl
Innerchr20:23559359..23889868hg18UCSC Ensembl
Cytoband20p11.21
Allele length
AssemblyAllele length
hg38330510
hg19330510
hg18330510
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3893322
Supporting Variants
Samples
Known GenesCST1, CST2, CST3, CST4, CST5
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=71
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25791467
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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