A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2678934



Internal ID9945039
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:36075820..36077284hg38UCSC Ensembl
Outerchr20:36075783..36077334hg38UCSC Ensembl
Innerchr20:34663742..34665206hg19UCSC Ensembl
Outerchr20:34663705..34665256hg19UCSC Ensembl
Cytoband20q11.23
Allele length
AssemblyAllele length
hg381552
hg191552
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5451377
SamplesNA19474
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2678934
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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