A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5994167



Internal ID21903510
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:59413609..59413661hg38UCSC Ensembl
chr3:59399335..59399387hg19UCSC Ensembl
Cytoband3p14.2
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17550853
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5994167
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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