A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17159843



Internal ID21451488
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:113453315..113453315hg38UCSC Ensembl
chr9:116215595..116215595hg19UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg3872
hg1972
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5638046
Supporting Variants
SamplesHG01505
Known GenesRGS3
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17159843
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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