A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5558534



Internal ID331593
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:11285958..11597527hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg38311570
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17727374
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5558534
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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