A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17733592



Internal ID157258
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:62632193..62634445hg38UCSC Ensembl
chr20:61263545..61265797hg19UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg382253
hg192253
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5523896
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17733592
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000937


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