A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17596634



Internal ID21788677
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:113569593..113569593hg38UCSC Ensembl
chr9:116331873..116331873hg19UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6091776
Supporting Variants
Samples
Known GenesRGS3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17596634
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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