A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2669332



Internal ID9935437
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:9486159..9488299hg38UCSC Ensembl
chr20:9466806..9468946hg19UCSC Ensembl
Cytoband20p12.2
Allele length
AssemblyAllele length
hg382141
hg192141
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5624317
SamplesNA19317
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2669332
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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