A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17026934



Internal ID85677
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:101419833..101420140hg38UCSC Ensembl
chr9:104182115..104182422hg19UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg38308
hg19308
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5491516
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17026934
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.067407


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