A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893309



Internal ID18837443
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:14799673..14903655hg38UCSC Ensembl
Outerchr20:14799673..14903655hg38UCSC Ensembl
Innerchr20:14780319..14884301hg19UCSC Ensembl
Outerchr20:14780319..14884301hg19UCSC Ensembl
Innerchr20:14728319..14832301hg18UCSC Ensembl
Outerchr20:14728319..14832301hg18UCSC Ensembl
Cytoband20p12.1
Allele length
AssemblyAllele length
hg38103983
hg19103983
hg18103983
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25796062
Samples
Known GenesMACROD2, MACROD2-AS1
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893309
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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