A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5883197



Internal ID22658175
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:35905909..35910380hg38UCSC Ensembl
chr19:36396811..36401282hg19UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg384472
hg194472
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17475255
Samples
Known GenesTYROBP
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5883197
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