A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25778349



Internal ID18819108
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:14884242..15036594hg38UCSC Ensembl
Innerchr20:14864888..15017240hg19UCSC Ensembl
Innerchr20:14812888..14965240hg18UCSC Ensembl
Cytoband20p12.1
Allele length
AssemblyAllele length
hg38152353
hg19152353
hg18152353
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=39
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25778349
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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