A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15967926



Internal ID19693180
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:39165521..39346363hg38UCSC Ensembl
chr22:39561526..39742368hg19UCSC Ensembl
Cytoband22q13.1
Allele length
AssemblyAllele length
hg38180843
hg19180843
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4291844
Supporting Variants
Samples
Known GenesPDGFB, RNU86, RPL3, SNORD43, SNORD83A, SNORD83B
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)nssv15967926
Frequency
Sample Size10847
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000046


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