A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893353



Internal ID19184173
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:60441669..60571638hg38UCSC Ensembl
Outerchr20:60441669..60571638hg38UCSC Ensembl
Innerchr20:59016727..59146696hg19UCSC Ensembl
Outerchr20:59016727..59146696hg19UCSC Ensembl
Innerchr20:58450122..58580091hg18UCSC Ensembl
Outerchr20:58450122..58580091hg18UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg38129970
hg19129970
hg18129970
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25792833
Samples
Known GenesMIR4533
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893353
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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