A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5557568



Internal ID330663
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:86614295..86661273hg38UCSC Ensembl
chr9:89229210..89276188hg19UCSC Ensembl
Cytoband9q21.33
Allele length
AssemblyAllele length
hg3846979
hg1946979
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17023894
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5557568
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