A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893135



Internal ID18837269
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:69878044..69889410hg38UCSC Ensembl
Outerchr18:69877481..69889410hg38UCSC Ensembl
Innerchr18:67545280..67556646hg19UCSC Ensembl
Outerchr18:67544717..67556646hg19UCSC Ensembl
Innerchr18:65696260..65707626hg18UCSC Ensembl
Outerchr18:65695697..65707626hg18UCSC Ensembl
Cytoband18q22.2
Allele length
AssemblyAllele length
hg3811930
hg1911930
hg1811930
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25801039, essv25799464, essv25779754, essv25785508, essv25785549, essv25784208, essv25784040, essv25780729, essv25786108, essv25801033
Samples
Known GenesCD226
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893135
Frequency
Sample Size3017
Observed Gain0
Observed Loss10
Observed Complex0
Frequencyn/a


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