A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17026668



Internal ID85512
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:107944397..107944458hg38UCSC Ensembl
chr9:110706678..110706739hg19UCSC Ensembl
Cytoband9q31.2
Allele length
AssemblyAllele length
hg3862
hg1962
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5482443
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17026668
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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