A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17691123



Internal ID114789
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:89358979..89368979hg38UCSC Ensembl
chr13:90011233..90021233hg19UCSC Ensembl
Cytoband13q31.3
Allele length
AssemblyAllele length
hg3810001
hg1910001
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5510935
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17691123
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000625


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