A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17854356



Internal ID22037999
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:94119020..94119020hg38UCSC Ensembl
chr3:93837864..93837864hg19UCSC Ensembl
Cytoband3q11.1
Allele length
AssemblyAllele length
hg38281
hg19281
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6254337
Supporting Variants
Samples
Known GenesNSUN3
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17854356
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