A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5981681



Internal ID21891024
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:167581919..167593959hg38UCSC Ensembl
chr1:167551156..167563196hg19UCSC Ensembl
Cytoband1q24.2
Allele length
AssemblyAllele length
hg3812041
hg1912041
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17536559
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5981681
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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