A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4233907



Internal ID20433400
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:74031668..74542994hg38UCSC Ensembl
chr16:74065567..74576892hg19UCSC Ensembl
Cytoband16q22.3
Allele length
AssemblyAllele length
hg38511327
hg19511326
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15955046
Samples
Known GenesCLEC18B, GLG1, LOC101928035, LOC283922, PSMD7
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 ID32461652
Accession Number(s)nsv4233907
Frequency
Sample Size10847
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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