A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2666568



Internal ID9932673
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:176333786..176334940hg38UCSC Ensembl
Outerchr3:176333752..176334975hg38UCSC Ensembl
Innerchr3:176051574..176052728hg19UCSC Ensembl
Outerchr3:176051540..176052763hg19UCSC Ensembl
Cytoband3q26.32
Allele length
AssemblyAllele length
hg381224
hg191224
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5844931
SamplesHG00108
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2666568
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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