A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893133



Internal ID19183953
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:69259177..69355381hg38UCSC Ensembl
Outerchr18:69259177..69355381hg38UCSC Ensembl
Innerchr18:66926413..67022617hg19UCSC Ensembl
Outerchr18:66926413..67022617hg19UCSC Ensembl
Innerchr18:65077393..65173597hg18UCSC Ensembl
Outerchr18:65077393..65173597hg18UCSC Ensembl
Cytoband18q22.2
Allele length
AssemblyAllele length
hg3896205
hg1996205
hg1896205
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25791968
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893133
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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