A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17693364



Internal ID117030
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:80368804..80369177hg38UCSC Ensembl
chr13:80942939..80943312hg19UCSC Ensembl
Cytoband13q31.1
Allele length
AssemblyAllele length
hg38374
hg19374
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6143314
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17693364
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.149847


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