A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17094902



Internal ID21451507
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:86380549..86380549hg38UCSC Ensembl
chr16:86414155..86414155hg19UCSC Ensembl
Cytoband16q24.1
Allele length
AssemblyAllele length
hg38742
hg19742
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5655887
Supporting Variants
SamplesHG01505
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17094902
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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