A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17371389



Internal ID22597058
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:89860057..89893275hg38UCSC Ensembl
chr16:89926465..89959683hg19UCSC Ensembl
Cytoband16q24.3
Allele length
AssemblyAllele length
hg3833219
hg1933219
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5928506
Supporting Variants
Samples
Known GenesSPIRE2, TCF25
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17371389
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.001


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