A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17027087



Internal ID85778
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:108982713..108983270hg38UCSC Ensembl
chr9:111744993..111745550hg19UCSC Ensembl
Cytoband9q31.3
Allele length
AssemblyAllele length
hg38558
hg19558
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5478027
Supporting Variants
Samples
Known GenesCTNNAL1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17027087
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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