A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17163279



Internal ID21508867
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:99084645..99084645hg38UCSC Ensembl
chr9:101846927..101846927hg19UCSC Ensembl
Cytoband9q22.33
Allele length
AssemblyAllele length
hg3813713
hg1913713
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5628735
Supporting Variants
SamplesNA20847
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17163279
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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