A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5493377



Internal ID270561
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:14498765..14498825hg38UCSC Ensembl
chr9:14498763..14498823hg19UCSC Ensembl
Cytoband9p22.3
Allele length
AssemblyAllele length
hg3861
hg1961
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17019098
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5493377
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