A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5561137



Internal ID334124
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:105859426..106651185hg38UCSC Ensembl
chr3:105578270..106370032hg19UCSC Ensembl
Cytoband3q13.11
Allele length
AssemblyAllele length
hg38791760
hg19791763
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16937241
Samples
Known GenesCBLB
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5561137
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