A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2659454



Internal ID9925559
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:51890446..51893083hg38UCSC Ensembl
Outerchr20:51890409..51893133hg38UCSC Ensembl
Innerchr20:50506985..50509622hg19UCSC Ensembl
Outerchr20:50506948..50509672hg19UCSC Ensembl
Cytoband20q13.2
Allele length
AssemblyAllele length
hg382725
hg192725
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5502727
SamplesNA18541
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2659454
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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