A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5991372



Internal ID21900715
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:132390823..132391936hg38UCSC Ensembl
chr3:132109667..132110780hg19UCSC Ensembl
Cytoband3q22.1
Allele length
AssemblyAllele length
hg381114
hg191114
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17544576
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5991372
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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