A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5936146



Internal ID22711497
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:32446697..32448563hg38UCSC Ensembl
chr19:32937603..32939469hg19UCSC Ensembl
Cytoband19q13.11
Allele length
AssemblyAllele length
hg381867
hg191867
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17400721
Samples
Known GenesDPY19L3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5936146
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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