A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5991951



Internal ID21901294
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:165196896..165196957hg38UCSC Ensembl
chr3:164914684..164914745hg19UCSC Ensembl
Cytoband3q26.1
Allele length
AssemblyAllele length
hg3862
hg1962
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17542967
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5991951
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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