A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17028538



Internal ID86722
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:121250394..121250727hg38UCSC Ensembl
chr9:124012672..124013005hg19UCSC Ensembl
Cytoband9q33.2
Allele length
AssemblyAllele length
hg38334
hg19334
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5493116
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17028538
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000468


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer