A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5490361



Internal ID267618
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:93199955..93211224hg38UCSC Ensembl
chr8:94212184..94223453hg19UCSC Ensembl
Cytoband8q22.1
Allele length
AssemblyAllele length
hg3811270
hg1911270
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17013540
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5490361
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