A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5923224



Internal ID22698450
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:93444857..93449728hg38UCSC Ensembl
chr9:96207139..96212010hg19UCSC Ensembl
Cytoband9q22.31
Allele length
AssemblyAllele length
hg384872
hg194872
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17435646
Samples
Known GenesFAM120AOS
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5923224
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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