A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2658564



Internal ID9924669
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:33468078..33476489hg38UCSC Ensembl
Outerchr20:33468041..33476539hg38UCSC Ensembl
Innerchr20:32055884..32064295hg19UCSC Ensembl
Outerchr20:32055847..32064345hg19UCSC Ensembl
Cytoband20q11.21
Allele length
AssemblyAllele length
hg388499
hg198499
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6350665
SamplesNA18565
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2658564
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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