A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5486331



Internal ID263700
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:11732342..12015977hg38UCSC Ensembl
chr9:11732342..12015977hg19UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg38283636
hg19283636
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv524n206
Supporting Variantsnssv17022268
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5486331
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