A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5475246



Internal ID252890
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:20335381..20363231hg38UCSC Ensembl
chr8:20192892..20220742hg19UCSC Ensembl
Cytoband8p21.3
Allele length
AssemblyAllele length
hg3827851
hg1927851
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17009153
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5475246
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