A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17162999



Internal ID21428894
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:76304530..76306923hg38UCSC Ensembl
chr9:78919446..78921839hg19UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg382394
hg192394
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5601755
Supporting Variants
SamplesHG00731
Known GenesPCSK5
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17162999
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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