A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2671820



Internal ID9937925
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:109060001..109061868hg38UCSC Ensembl
Outerchr8:109059844..109062021hg38UCSC Ensembl
Innerchr8:110072230..110074097hg19UCSC Ensembl
Outerchr8:110072073..110074250hg19UCSC Ensembl
Cytoband8q23.1
Allele length
AssemblyAllele length
hg382178
hg192178
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5721238
SamplesNA19440
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2671820
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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