A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25782484



Internal ID18821797
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:14884242..15098078hg38UCSC Ensembl
Innerchr20:14864888..15078724hg19UCSC Ensembl
Innerchr20:14812888..15026724hg18UCSC Ensembl
Cytoband20p12.1
Allele length
AssemblyAllele length
hg38213837
hg19213837
hg18213837
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 HumanHap 610
CommentsNumber of probes=73
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25782484
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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