A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4747352



Internal ID20523370
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:36126349..36126755hg38UCSC Ensembl
chr22:36522397..36522803hg19UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg38407
hg19407
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16261524
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4747352
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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