A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6007219



Internal ID21916562
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:76214610..76215715hg38UCSC Ensembl
chr9:78829526..78830631hg19UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg381106
hg191106
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17587798
Samples
Known GenesPCSK5
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6007219
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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