A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5485256



Internal ID262652
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:101467117..101469406hg38UCSC Ensembl
chr8:102479345..102481634hg19UCSC Ensembl
Cytoband8q22.3
Allele length
AssemblyAllele length
hg382290
hg192290
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17014782
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5485256
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