A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4741273



Internal ID20517250
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:43404190..43404247hg38UCSC Ensembl
chr22:43800196..43800253hg19UCSC Ensembl
Cytoband22q13.2
Allele length
AssemblyAllele length
hg3858
hg1958
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16260839
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4741273
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