A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5492630



Internal ID269839
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:97076668..97083616hg38UCSC Ensembl
chr9:99838950..99845898hg19UCSC Ensembl
Cytoband9q22.33
Allele length
AssemblyAllele length
hg386949
hg196949
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17027528
Samples
Known GenesLOC340508
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5492630
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