A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6050244



Internal ID21959477
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:35005164..35005232hg38UCSC Ensembl
chr22:35401154..35401222hg19UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg3869
hg1969
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17649433
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6050244
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