A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17845183



Internal ID22028826
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:36083033..36083033hg38UCSC Ensembl
chr13:36657170..36657170hg19UCSC Ensembl
Cytoband13q13.3
Allele length
AssemblyAllele length
hg38272
hg19272
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6248907
Supporting Variants
Samples
Known GenesDCLK1
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17845183
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