A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17160093



Internal ID21401344
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:126013156..126013156hg38UCSC Ensembl
chr9:128775435..128775435hg19UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg38114
hg19114
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5636118
Supporting Variants
SamplesHG00096
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17160093
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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