A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3555675



Internal ID18756751
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:75559731..75560121hg38UCSC Ensembl
Outerchr18:75559713..75560217hg38UCSC Ensembl
Innerchr18:73271686..73272076hg19UCSC Ensembl
Outerchr18:73271668..73272172hg19UCSC Ensembl
Cytoband18q23
Allele length
AssemblyAllele length
hg38505
hg19505
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv209e215
Supporting Variantsessv9754422
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3555675
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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