A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4764284



Internal ID20540144
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:24813584..24813584hg38UCSC Ensembl
chr3:24855075..24855075hg19UCSC Ensembl
Cytoband3p24.2
Allele length
AssemblyAllele length
hg3859
hg1959
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16293493
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4764284
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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