A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4733396



Internal ID20509326
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:79957583..79958616hg38UCSC Ensembl
chr8:80869818..80870851hg19UCSC Ensembl
Cytoband8q21.13
Allele length
AssemblyAllele length
hg381034
hg191034
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16286237
Samples
Known GenesMRPS28
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4733396
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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