A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2660367



Internal ID9926472
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:60553033..60555557hg38UCSC Ensembl
chr20:59128091..59130615hg19UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg382525
hg192525
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5851869, essv5781212, essv5730674, essv6012835, essv6329762
SamplesNA18602, NA18973, HG00560, NA18538, HG00513
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2660367
Frequency
Sample Size1151
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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