A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893132



Internal ID19183952
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:69167846..69234778hg38UCSC Ensembl
Outerchr18:69167846..69235288hg38UCSC Ensembl
Innerchr18:66835083..66902015hg19UCSC Ensembl
Outerchr18:66835083..66902525hg19UCSC Ensembl
Innerchr18:64986063..65052995hg18UCSC Ensembl
Outerchr18:64986063..65053505hg18UCSC Ensembl
Cytoband18q22.2
Allele length
AssemblyAllele length
hg3867443
hg1967443
hg1867443
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25782500, essv25798077
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Illumina Human OmniExpress
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893132
Frequency
Sample Size3017
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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