A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5989282



Internal ID21898625
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:42997133..42997615hg38UCSC Ensembl
chr2:43224273..43224755hg19UCSC Ensembl
Cytoband2p21
Allele length
AssemblyAllele length
hg38483
hg19483
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17527156
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5989282
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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