A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5641483



Internal ID8618886
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 StatusS
Merged Variantsesv2678302
Supporting Variants
SamplesNA20771
Known GenesNSUN3
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5641483
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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