A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17021940



Internal ID82288
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:23404085..23599492hg38UCSC Ensembl
chr9:23404083..23599490hg19UCSC Ensembl
Cytoband9p21.3
Allele length
AssemblyAllele length
hg38195408
hg19195408
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5554806
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17021940
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000312


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