A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4758562



Internal ID20534422
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:14396786..14396786hg38UCSC Ensembl
chr3:14438286..14438286hg19UCSC Ensembl
Cytoband3p25.1
Allele length
AssemblyAllele length
hg38503
hg19503
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16261399
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4758562
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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