A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893078



Internal ID18837212
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:25391998..26039471hg38UCSC Ensembl
Outerchr18:25391998..26039471hg38UCSC Ensembl
Innerchr18:22971962..23619435hg19UCSC Ensembl
Outerchr18:22971962..23619435hg19UCSC Ensembl
Innerchr18:21225960..21873433hg18UCSC Ensembl
Outerchr18:21225960..21873433hg18UCSC Ensembl
Cytoband18q11.2
Allele length
AssemblyAllele length
hg38647474
hg19647474
hg18647474
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25791345
Samples
Known GenesSS18
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893078
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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