A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5991498



Internal ID21900841
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:129389268..129389416hg38UCSC Ensembl
chr3:129108111..129108259hg19UCSC Ensembl
Cytoband3q21.3
Allele length
AssemblyAllele length
hg38149
hg19149
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17543039
Samples
Known GenesRPL32P3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5991498
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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