A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17638092



Internal ID21830139
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:38160604..38165631hg38UCSC Ensembl
chr22:38556611..38561638hg19UCSC Ensembl
Cytoband22q13.1
Allele length
AssemblyAllele length
hg385028
hg195028
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6046187
Supporting Variants
Samples
Known GenesPLA2G6
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17638092
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