A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5991599



Internal ID21900942
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:148849005..148849323hg38UCSC Ensembl
chr3:148566792..148567110hg19UCSC Ensembl
Cytoband3q24
Allele length
AssemblyAllele length
hg38319
hg19319
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17548071
Samples
Known GenesCPB1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5991599
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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