A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4740844



Internal ID20516821
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:32520357..32521667hg38UCSC Ensembl
chr22:32916344..32917654hg19UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg381311
hg191311
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16274260
Samples
Known GenesSYN3
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4740844
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