A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5990711



Internal ID21900054
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:10035..10883hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg38849
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17529232
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5990711
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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