A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893296



Internal ID18837430
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:14725970..14874289hg38UCSC Ensembl
Outerchr20:14691531..14903655hg38UCSC Ensembl
Innerchr20:14706616..14854935hg19UCSC Ensembl
Outerchr20:14672177..14884301hg19UCSC Ensembl
Innerchr20:14654616..14802935hg18UCSC Ensembl
Outerchr20:14620177..14832301hg18UCSC Ensembl
Cytoband20p12.1
Allele length
AssemblyAllele length
hg38212125
hg19212125
hg18212125
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25784444, essv25782161, essv25782354, essv25778256, essv25783970, essv25801670
Samples
Known GenesMACROD2, MACROD2-AS1
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893296
Frequency
Sample Size3017
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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