A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5990748



Internal ID21900091
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:108543528..108547946hg38UCSC Ensembl
chr3:108262375..108266793hg19UCSC Ensembl
Cytoband3q13.13
Allele length
AssemblyAllele length
hg384419
hg194419
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17541364
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5990748
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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