A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17083914



Internal ID21401619
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:87344914..87344914hg38UCSC Ensembl
chr16:87378520..87378520hg19UCSC Ensembl
Cytoband16q24.2
Allele length
AssemblyAllele length
hg38175
hg19175
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5653973
Supporting Variants
SamplesHG00096
Known GenesFBXO31
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17083914
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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