A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17549763



Internal ID21874118
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:142608890..142612656hg38UCSC Ensembl
chr3:142327732..142331498hg19UCSC Ensembl
Cytoband3q23
Allele length
AssemblyAllele length
hg383767
hg193767
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5991410
Supporting Variants
Samples
Known GenesPLS1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17549763
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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