A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5992056



Internal ID21901399
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:145618549..145627776hg38UCSC Ensembl
chr3:145336336..145345563hg19UCSC Ensembl
Cytoband3q24
Allele length
AssemblyAllele length
hg389228
hg199228
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17551556
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5992056
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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