A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6040606



Internal ID21949949
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:21668923..21668995hg38UCSC Ensembl
chr22:22023212..22023284hg19UCSC Ensembl
Cytoband22q11.21
Allele length
AssemblyAllele length
hg3873
hg1973
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17639702
Samples
Known GenesPPIL2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6040606
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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