A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5561909



Internal ID334876
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:58574072..58575503hg38UCSC Ensembl
chr14:59040790..59042221hg19UCSC Ensembl
Cytoband14q23.1
Allele length
AssemblyAllele length
hg381432
hg191432
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17695884
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5561909
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