A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5483508



Internal ID260944
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:131320626..131326617hg38UCSC Ensembl
chr9:134196013..134202004hg19UCSC Ensembl
Cytoband9q34.13
Allele length
AssemblyAllele length
hg385992
hg195992
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17029864
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5483508
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