A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17732333



Internal ID155999
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:38870492..38871358hg38UCSC Ensembl
chr20:37499135..37500001hg19UCSC Ensembl
Cytoband20q11.23
Allele length
AssemblyAllele length
hg38867
hg19867
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5521405
Supporting Variants
Samples
Known GenesPPP1R16B
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17732333
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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