A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17162989



Internal ID21405263
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:76063888..76063888hg38UCSC Ensembl
chr9:78678804..78678804hg19UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg38178
hg19178
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5633475
Supporting Variants
SamplesHG00512
Known GenesPCSK5
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17162989
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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