A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893299



Internal ID19184119
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:14909565..15050398hg38UCSC Ensembl
Outerchr20:14884242..15140917hg38UCSC Ensembl
Innerchr20:14890211..15031044hg19UCSC Ensembl
Outerchr20:14864888..15121563hg19UCSC Ensembl
Innerchr20:14838211..14979044hg18UCSC Ensembl
Outerchr20:14812888..15069563hg18UCSC Ensembl
Cytoband20p12.1
Allele length
AssemblyAllele length
hg38256676
hg19256676
hg18256676
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25798056, essv25799084, essv25797045, essv25780832, essv25796374, essv25782484, essv25778349
Samples
Known GenesMACROD2, MACROD2-AS1
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Illumina Human OmniExpress
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893299
Frequency
Sample Size3017
Observed Gain0
Observed Loss7
Observed Complex0
Frequencyn/a


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