A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5463920



Internal ID241810
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:158998337..158998575hg38UCSC Ensembl
chr6:159419369..159419607hg19UCSC Ensembl
Cytoband6q25.3
Allele length
AssemblyAllele length
hg38239
hg19239
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16989553
Samples
Known GenesRSPH3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5463920
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