A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15954945



Internal ID19680199
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:67839746..67851424hg38UCSC Ensembl
chr16:67873649..67885327hg19UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg3811679
hg1911679
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4238173
Supporting Variants
Samples
Known GenesCENPT, NUTF2, THAP11
MethodSequencing
AnalysisSV calls were generated using multi-algorithm consensus pipeline involving raw evidence assessment, filtering, clustering, genotyping, alternative allele structure resolution, and gene annotation. These methods are described in detail in the gnomAD-SV preprint [Collins*, Brand*, et al., bioRxiv (2019)|https://www.biorxiv.org/content/10.1101/578674v1], and are largely based on methods developed in [Werling et al., Nat. Genet. (2018)|https://www.ncbi.nlm.nih.gov/pubmed/29700473].
Platform
Comments
ReferencegnomAD_Structural_Variants
Pubmed ID12345678
Accession Number(s)nssv15954945
Frequency
Sample Size10847
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000553


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