A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17086985



Internal ID21477007
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:67046743..67046743hg38UCSC Ensembl
chr16:67080646..67080646hg19UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg38339
hg19339
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5652323
Supporting Variants
SamplesHG03486
Known GenesCBFB
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17086985
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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