A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17586394



Internal ID21778437
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 StatusS
Merged Variantsnsv6009166
Supporting Variants
Samples
Known GenesPCSK5
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17586394
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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