A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4745650



Internal ID20521660
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:32771856..32771942hg38UCSC Ensembl
chr21:34144167..34144253hg19UCSC Ensembl
Cytoband21q22.11
Allele length
AssemblyAllele length
hg3887
hg1987
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16263378
Samples
Known GenesPAXBP1
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4745650
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