A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17644095



Internal ID21836142
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:31114978..31115032hg38UCSC Ensembl
chr22:31510964..31511018hg19UCSC Ensembl
Cytoband22q12.2
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6043912
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17644095
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