A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6009166



Internal ID21918509
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:76121810..76122122hg38UCSC Ensembl
chr9:78736726..78737038hg19UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg38313
hg19313
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17586394
Samples
Known GenesPCSK5
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6009166
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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