A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16293848



Internal ID20503066
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:114324100..114330877hg38UCSC Ensembl
chr9:117086380..117093157hg19UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg386778
hg196778
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4741220
Supporting Variants
Samples
Known GenesORM1, ORM2
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16293848
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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