A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5839519



Internal ID22614454
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:24796251..24799361hg38UCSC Ensembl
chr4:24797873..24800983hg19UCSC Ensembl
Cytoband4p15.2
Allele length
AssemblyAllele length
hg383111
hg193111
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17493377
Samples
Known GenesSOD3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5839519
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