A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17021062



Internal ID81680
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:7821332..7823468hg38UCSC Ensembl
chr9:7821332..7823468hg19UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg382137
hg192137
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5488049
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17021062
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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