A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893083



Internal ID18837217
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:27572120..27782257hg38UCSC Ensembl
Outerchr18:27572120..27782257hg38UCSC Ensembl
Innerchr18:25152084..25362221hg19UCSC Ensembl
Outerchr18:25152084..25362221hg19UCSC Ensembl
Innerchr18:23406082..23616219hg18UCSC Ensembl
Outerchr18:23406082..23616219hg18UCSC Ensembl
Cytoband18q12.1
Allele length
AssemblyAllele length
hg38210138
hg19210138
hg18210138
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25791346
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893083
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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