A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5482242



Internal ID259700
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:1199934..1406504hg38UCSC Ensembl
chr9:1199934..1406504hg19UCSC Ensembl
Cytoband9p24.3
Allele length
AssemblyAllele length
hg38206571
hg19206571
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv520n206
Supporting Variantsnssv17017783
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5482242
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