A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17163000



Internal ID21460437
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:76304530..76304795hg38UCSC Ensembl
chr9:78919446..78919711hg19UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg38266
hg19266
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5591777
Supporting Variants
SamplesHG02818
Known GenesPCSK5
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17163000
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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