A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4035426



Internal ID20165606
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:154165625..154240637hg38UCSC Ensembl
chrX:153431100..153506110hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg3875013
hg1975011
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15990447
Samples
Known GenesOPN1MW, OPN1MW2, TEX28
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)nsv4035426
Frequency
Sample Size10847
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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