A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16962939



Internal ID42621
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:18084798..18086372hg38UCSC Ensembl
chr5:18084907..18086481hg19UCSC Ensembl
Cytoband5p15.1
Allele length
AssemblyAllele length
hg381575
hg191575
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5556163
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16962939
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.001561


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