A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4268567



Internal ID20110396
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:46134382..46240987hg38UCSC Ensembl
chr19:46637639..46744244hg19UCSC Ensembl
Cytoband19q13.32
Allele length
AssemblyAllele length
hg38106606
hg19106606
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15961706
Samples
Known GenesDKFZp434J0226, IGFL1, IGFL2, RNU6-66P
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)nsv4268567
Frequency
Sample Size10847
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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