A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17841470



Internal ID22025113
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:76161457..76161457hg38UCSC Ensembl
chr9:78776373..78776373hg19UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg38279
hg19279
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6257772
Supporting Variants
Samples
Known GenesPCSK5
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17841470
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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