A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893124



Internal ID19183944
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:67950784..68111102hg38UCSC Ensembl
Outerchr18:67950784..68111102hg38UCSC Ensembl
Innerchr18:65618021..65778339hg19UCSC Ensembl
Outerchr18:65618021..65778339hg19UCSC Ensembl
Innerchr18:63769001..63929319hg18UCSC Ensembl
Outerchr18:63769001..63929319hg18UCSC Ensembl
Cytoband18q22.1
Allele length
AssemblyAllele length
hg38160319
hg19160319
hg18160319
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25786153
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893124
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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