A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25792833



Internal ID19177962
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:60441669..60571638hg38UCSC Ensembl
Innerchr20:59016727..59146696hg19UCSC Ensembl
Innerchr20:58450122..58580091hg18UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg38129970
hg19129970
hg18129970
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3893353
Supporting Variants
Samples
Known GenesMIR4533
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=41
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25792833
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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