A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2661960



Internal ID9928065
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:32871117..32874186hg38UCSC Ensembl
chr20:31458923..31461992hg19UCSC Ensembl
Cytoband20q11.21
Allele length
AssemblyAllele length
hg383070
hg193070
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6220923, essv5523528, essv6143157, essv5410202, essv6321829, essv5885673
SamplesNA19701, NA19374, NA19712, NA19376, NA19472, NA19093
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2661960
Frequency
Sample Size1151
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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