A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5981069



Internal ID21890412
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:143206034..143208678hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg382645
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17532154
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5981069
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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