A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5479063



Internal ID256602
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:114398142..114399187hg38UCSC Ensembl
chr9:117160422..117161467hg19UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg381046
hg191046
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17028369
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5479063
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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