A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6541627



Internal ID20914909
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:18060977..18064035hg38UCSC Ensembl
chr22:18543743..18546801hg19UCSC Ensembl
Cytoband22q11.21
Allele length
AssemblyAllele length
hg383059
hg193059
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18072867
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6541627
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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