A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5485792



Internal ID263174
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 StatusM
Merged Variants
Supporting Variantsnssv17027089
Samples
Known GenesCTNNAL1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5485792
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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