A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893278



Internal ID19184098
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:7184078..7377776hg38UCSC Ensembl
Outerchr20:7184078..7377776hg38UCSC Ensembl
Innerchr20:7164725..7358423hg19UCSC Ensembl
Outerchr20:7164725..7358423hg19UCSC Ensembl
Innerchr20:7112725..7306423hg18UCSC Ensembl
Outerchr20:7112725..7306423hg18UCSC Ensembl
Cytoband20p12.3
Allele length
AssemblyAllele length
hg38193699
hg19193699
hg18193699
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25785399
Samples
Known GenesMIR8062
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893278
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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