A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25788384



Internal ID19167996
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:23701496..23746320hg38UCSC Ensembl
Innerchr20:23682133..23726957hg19UCSC Ensembl
Innerchr20:23630133..23674957hg18UCSC Ensembl
Cytoband20p11.21
Allele length
AssemblyAllele length
hg3844825
hg1944825
hg1844825
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3893321
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=13
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25788384
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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