A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5490235



Internal ID267496
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:100910264..100920111hg38UCSC Ensembl
chr9:103672546..103682393hg19UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg389848
hg199848
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17025044
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5490235
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