A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893314



Internal ID19184134
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:14878264..14925213hg38UCSC Ensembl
Outerchr20:14878264..14925213hg38UCSC Ensembl
Innerchr20:14858910..14905859hg19UCSC Ensembl
Outerchr20:14858910..14905859hg19UCSC Ensembl
Innerchr20:14806910..14853859hg18UCSC Ensembl
Outerchr20:14806910..14853859hg18UCSC Ensembl
Cytoband20p12.1
Allele length
AssemblyAllele length
hg3846950
hg1946950
hg1846950
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25798975
Samples
Known GenesMACROD2, MACROD2-AS1
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893314
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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