A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17024154



Internal ID83831
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:66591387..66669450hg38UCSC Ensembl
chr9:41852503..41930502hg19UCSC Ensembl
Cytoband9p12
Allele length
AssemblyAllele length
hg3878064
hg1978000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6142070
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17024154
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.009005


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