A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17025634



Internal ID84824
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:87912552..87918700hg38UCSC Ensembl
chr9:90527467..90533615hg19UCSC Ensembl
Cytoband9q22.1
Allele length
AssemblyAllele length
hg386149
hg196149
Variant TypeOTHER copy number variation
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5414820
Supporting Variants
Samples
Known GenesSPATA31C1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17025634
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.492726


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