A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16276020



Internal ID20485238
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:93451378..93451451hg38UCSC Ensembl
chr9:96213660..96213733hg19UCSC Ensembl
Cytoband9q22.31
Allele length
AssemblyAllele length
hg3874
hg1974
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4735588
Supporting Variants
Samples
Known GenesFAM120AOS
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16276020
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer