A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17731441



Internal ID155107
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:19924136..19924511hg38UCSC Ensembl
chr20:19904780..19905155hg19UCSC Ensembl
Cytoband20p11.23
Allele length
AssemblyAllele length
hg38376
hg19376
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5519230
Supporting Variants
Samples
Known GenesRIN2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17731441
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.813086


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