A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18072598



Internal ID20639638
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:21668052..21669124hg38UCSC Ensembl
chr22:22022341..22023413hg19UCSC Ensembl
Cytoband22q11.21
Allele length
AssemblyAllele length
hg381073
hg191073
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6552927
Supporting Variants
Samples
Known GenesPPIL2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18072598
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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