A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17022736



Internal ID82845
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:76790552..76815552hg38UCSC Ensembl
chr9:79405468..79430468hg19UCSC Ensembl
Cytoband9q21.2
Allele length
AssemblyAllele length
hg3825001
hg1925001
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5489646
Supporting Variants
Samples
Known GenesPRUNE2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17022736
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000625


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