Variant DetailsVariant: nsv4049134 | Internal ID | 20175162 | | Landmark | | | Location Information | | | Cytoband | Xq11.1 | | Allele length | | Assembly | Allele length | | hg38 | 13288 | | hg19 | 13289 |
| | Variant Type | OTHER complex | | Copy Number | | | Allele State | | | Allele Origin | | | Probe Count | | | Validation Flag | | | Merged Status | M | | Merged Variants | | | Supporting Variants | nssv15786380, nssv15786419, nssv15786377, nssv15786372, nssv15786374, nssv15786389, nssv15786391, nssv15786390, nssv15786373, nssv15786411, nssv15786381, nssv15786420, nssv15786415, nssv15786406, nssv15786413, nssv15786395, nssv15786386, nssv15786401, nssv15786385, nssv15786392, nssv15786405, nssv15786396, nssv15786409, nssv15786400, nssv15786418, nssv15786394, nssv15786422, nssv15786384, nssv15786416, nssv15786371, nssv15786403, nssv15786382, nssv15786404, nssv15786399, nssv15786379, nssv15786397, nssv15786425, nssv15786387, nssv15786421, nssv15786375, nssv15786407, nssv15786423, nssv15786412, nssv15786376, nssv15786410, nssv15786398, nssv15786408, nssv15786378, nssv15786414, nssv15786424, nssv15786393, nssv15786402, nssv15786388, nssv15786417, nssv15786383 | | Samples | | | Known Genes | | | Method | Sequencing | | Analysis | SV 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 | | | Reference | gnomAD_Structural_Variants | | Pubmed ID | 32461652 | | Accession Number(s) | nsv4049134
| | Frequency | | Sample Size | 10847 | | Observed Gain | 0 | | Observed Loss | 0 | | Observed Complex | 0 | | Frequency | n/a |
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