A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25798056



Internal ID18824335
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:14886582..15050398hg38UCSC Ensembl
Innerchr20:14867228..15031044hg19UCSC Ensembl
Innerchr20:14815228..14979044hg18UCSC Ensembl
Cytoband20p12.1
Allele length
AssemblyAllele length
hg38163817
hg19163817
hg18163817
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=40
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25798056
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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