A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5991596



Internal ID21900939
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:148594641..148598280hg38UCSC Ensembl
chr3:148312428..148316067hg19UCSC Ensembl
Cytoband3q24
Allele length
AssemblyAllele length
hg383640
hg193640
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17539846
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5991596
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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