A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5835554



Internal ID22610489
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:24128161..24129186hg38UCSC Ensembl
chr3:24169652..24170677hg19UCSC Ensembl
Cytoband3p24.2
Allele length
AssemblyAllele length
hg381026
hg191026
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17490539
Samples
Known GenesTHRB
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5835554
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