A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17541563



Internal ID21865918
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:146164376..146164464hg38UCSC Ensembl
chr3:145882163..145882251hg19UCSC Ensembl
Cytoband3q24
Allele length
AssemblyAllele length
hg3889
hg1989
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5991650
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17541563
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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