A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17585516



Internal ID21777559
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:107293001..107293001hg38UCSC Ensembl
chr9:110055282..110055282hg19UCSC Ensembl
Cytoband9q31.2
Allele length
AssemblyAllele length
hg38236
hg19236
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6094655
Supporting Variants
Samples
Known GenesRAD23B
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17585516
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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