A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18204951



Internal ID20771991
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:26991938..27005049hg38UCSC Ensembl
chr22:27387901..27401012hg19UCSC Ensembl
Cytoband22q12.1
Allele length
AssemblyAllele length
hg3813112
hg1913112
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6543165
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18204951
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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