A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5560305



Internal ID333315
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 StatusM
Merged Variants
Supporting Variantsnssv17732197
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)nsv5560305
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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