A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25797045



Internal ID18830928
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:14899681..15098078hg38UCSC Ensembl
Innerchr20:14880327..15078724hg19UCSC Ensembl
Innerchr20:14828327..15026724hg18UCSC Ensembl
Cytoband20p12.1
Allele length
AssemblyAllele length
hg38198398
hg19198398
hg18198398
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3893299
Supporting Variants
Samples
Known GenesMACROD2, MACROD2-AS1
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
CommentsNumber of probes=59
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25797045
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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