A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17597288



Internal ID21789331
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:113453184..113453269hg38UCSC Ensembl
chr9:116215464..116215549hg19UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg3886
hg1986
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6016207
Supporting Variants
Samples
Known GenesRGS3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17597288
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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