A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893097



Internal ID18837231
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:41680652..42201288hg38UCSC Ensembl
Outerchr18:41680652..42201288hg38UCSC Ensembl
Innerchr18:39260616..39781253hg19UCSC Ensembl
Outerchr18:39260616..39781253hg19UCSC Ensembl
Innerchr18:37514614..38035251hg18UCSC Ensembl
Outerchr18:37514614..38035251hg18UCSC Ensembl
Cytoband18q12.3
Allele length
AssemblyAllele length
hg38520637
hg19520638
hg18520638
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25790770
Samples
Known GenesLINC00907, PIK3C3
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893097
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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