A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5489123



Internal ID266412
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:93408273..93449985hg38UCSC Ensembl
chr9:96170555..96212267hg19UCSC Ensembl
Cytoband9q22.31
Allele length
AssemblyAllele length
hg3841713
hg1941713
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17025702
Samples
Known GenesFAM120AOS
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5489123
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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