A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17439173



Internal ID22497043
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:107293084..107293133hg38UCSC Ensembl
chr9:110055365..110055414hg19UCSC Ensembl
Cytoband9q31.2
Allele length
AssemblyAllele length
hg3850
hg1950
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5923331
Supporting Variants
Samples
Known GenesRAD23B
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17439173
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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