A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5994446



Internal ID21903789
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:71659515..71660068hg38UCSC Ensembl
chr3:71708666..71709219hg19UCSC Ensembl
Cytoband3p13
Allele length
AssemblyAllele length
hg38554
hg19554
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17556984
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5994446
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer