A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17733063



Internal ID156729
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:53686979..53721922hg38UCSC Ensembl
chr20:52303518..52338461hg19UCSC Ensembl
Cytoband20q13.2
Allele length
AssemblyAllele length
hg3834944
hg1934944
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5532532
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17733063
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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