A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5982096



Internal ID21891439
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:198356590..198359481hg38UCSC Ensembl
chr1:198325720..198328611hg19UCSC Ensembl
Cytoband1q31.3
Allele length
AssemblyAllele length
hg382892
hg192892
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17528759
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5982096
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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