A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5839828



Internal ID22614763
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:86163508..86166047hg38UCSC Ensembl
chr4:87084661..87087200hg19UCSC Ensembl
Cytoband4q21.3
Allele length
AssemblyAllele length
hg382540
hg192540
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17497903
Samples
Known GenesMAPK10
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5839828
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