A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5554459



Internal ID327645
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:108000975..108023284hg38UCSC Ensembl
chr3:107719822..107742131hg19UCSC Ensembl
Cytoband3q13.12
Allele length
AssemblyAllele length
hg3822310
hg1922310
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16937543
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5554459
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