A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17738465



Internal ID162131
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:60519221..60522222hg38UCSC Ensembl
chr9_gl000199_random:663..3664hg19UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg383002
hg193002
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5478232
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17738465
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000312


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