A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5490097



Internal ID267359
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:9131204..9134391hg38UCSC Ensembl
chr8:8988714..8991901hg19UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg383188
hg193188
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17008682
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5490097
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