A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5981880



Internal ID21891223
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:158585335..158608315hg38UCSC Ensembl
chr1:158555125..158578105hg19UCSC Ensembl
Cytoband1q23.1
Allele length
AssemblyAllele length
hg3822981
hg1922981
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17524681
Samples
Known GenesOR10Z1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5981880
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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