A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17854494



Internal ID22038137
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:132487579..132487579hg38UCSC Ensembl
chr3:132206423..132206423hg19UCSC Ensembl
Cytoband3q22.1
Allele length
AssemblyAllele length
hg38268
hg19268
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6254686
Supporting Variants
Samples
Known GenesDNAJC13
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17854494
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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