A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17732132



Internal ID155798
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:34892894..34899048hg38UCSC Ensembl
chr20:33480697..33486851hg19UCSC Ensembl
Cytoband20q11.22
Allele length
AssemblyAllele length
hg386155
hg196155
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5520172
Supporting Variants
Samples
Known GenesACSS2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17732132
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