A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5885354



Internal ID22660338
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:35907609..35908880hg38UCSC Ensembl
chr19:36398511..36399782hg19UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg381272
hg191272
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17475257, nssv17475258
Samples
Known GenesTYROBP
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5885354
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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