A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5838480



Internal ID22613415
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:182546606..182548930hg38UCSC Ensembl
chr4:183467759..183470083hg19UCSC Ensembl
Cytoband4q35.1
Allele length
AssemblyAllele length
hg382325
hg192325
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17491309
Samples
Known GenesTENM3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5838480
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