A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893488



Internal ID18837622
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:43018324..43040163hg38UCSC Ensembl
Outerchr22:43018324..43040163hg38UCSC Ensembl
Innerchr22:43414330..43436169hg19UCSC Ensembl
Outerchr22:43414330..43436169hg19UCSC Ensembl
Innerchr22:41744274..41766113hg18UCSC Ensembl
Outerchr22:41744274..41766113hg18UCSC Ensembl
Cytoband22q13.2
Allele length
AssemblyAllele length
hg3821840
hg1921840
hg1821840
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25785874
Samples
Known GenesTTLL1
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893488
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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