A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2668606



Internal ID9934711
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:32928551..32931650hg38UCSC Ensembl
chr8:32786069..32789168hg19UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg383100
hg193100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5887774
SamplesHG01198
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2668606
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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