A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2660073



Internal ID9926178
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:109694794..109751412hg38UCSC Ensembl
chr8:110707023..110763641hg19UCSC Ensembl
Cytoband8q23.2
Allele length
AssemblyAllele length
hg3856619
hg1956619
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5578453
SamplesHG00367
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2660073
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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