A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4267108



Internal ID20109375
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:45618742..45647742hg38UCSC Ensembl
chr19:46122000..46151000hg19UCSC Ensembl
Cytoband19q13.32
Allele length
AssemblyAllele length
hg3829001
hg1929001
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15961693
Samples
Known GenesC19orf83, EML2, MIR330
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)nsv4267108
Frequency
Sample Size10847
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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