A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5457759



Internal ID235796
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:52901910..52922350hg38UCSC Ensembl
chr6:52766708..52787148hg19UCSC Ensembl
Cytoband6p12.2
Allele length
AssemblyAllele length
hg3820441
hg1920441
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16985917
Samples
Known GenesGSTA3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5457759
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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