A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17687395



Internal ID111061
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:45312168..45313208hg38UCSC Ensembl
chr13:45886303..45887343hg19UCSC Ensembl
Cytoband13q14.13
Allele length
AssemblyAllele length
hg381041
hg191041
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5563432
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17687395
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000781


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