A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17028315



Internal ID86569
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:113657506..113658369hg38UCSC Ensembl
chr9:116419786..116420649hg19UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg38864
hg19864
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5562008
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17028315
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000781


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