A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17732197



Internal ID155863
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:36507286..36660208hg38UCSC Ensembl
chr20:35135689..35288611hg19UCSC Ensembl
Cytoband20q11.23
Allele length
AssemblyAllele length
hg38152923
hg19152923
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5560305
Supporting Variants
Samples
Known GenesC20orf24, DLGAP4, MYL9, NDRG3, SLA2, TGIF2, TGIF2-C20orf24
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17732197
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000312


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