A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2678302



Internal ID9597721
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:94083509..94086563hg38UCSC Ensembl
Outerchr3:94083472..94086613hg38UCSC Ensembl
Innerchr3:93802353..93805407hg19UCSC Ensembl
Outerchr3:93802316..93805457hg19UCSC Ensembl
Cytoband3q11.1
Allele length
AssemblyAllele length
hg383142
hg193142
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5641483
SamplesNA20771
Known GenesNSUN3
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2678302
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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