A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2666081



Internal ID9932186
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:110017659..110019604hg38UCSC Ensembl
Outerchr8:110017622..110019654hg38UCSC Ensembl
Innerchr8:111029888..111031833hg19UCSC Ensembl
Outerchr8:111029851..111031883hg19UCSC Ensembl
Cytoband8q23.2
Allele length
AssemblyAllele length
hg382033
hg192033
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5632266
SamplesNA19338
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2666081
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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