A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17027398



Internal ID85981
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:92168218..92191457hg38UCSC Ensembl
chr9:94930500..94953739hg19UCSC Ensembl
Cytoband9q22.31
Allele length
AssemblyAllele length
hg3823240
hg1923240
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5478443
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17027398
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000312


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