A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17027089



Internal ID85780
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:108995846..108995963hg38UCSC Ensembl
chr9:111758126..111758243hg19UCSC Ensembl
Cytoband9q31.3
Allele length
AssemblyAllele length
hg38118
hg19118
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5485792
Supporting Variants
Samples
Known GenesCTNNAL1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17027089
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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