A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17556575



Internal ID21880930
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:133785399..133785454hg38UCSC Ensembl
chr3:133504243..133504298hg19UCSC Ensembl
Cytoband3q22.1
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5991315
Supporting Variants
Samples
Known GenesSRPRB
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17556575
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