Variant DetailsVariant: esv1007027Internal ID | 6719142 | Landmark | | Location Information | | Cytoband | Xq22.2 | Allele length | Assembly | Allele length | hg38 | 125524 | hg19 | 115636 | hg18 | 115636 |
| Variant Type | OTHER inversion | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | essv3564812 | Samples | HuRef | Known Genes | H2BFM, H2BFWT, H2BFXP, MIR1256, TMSB15B | Method | Sequencing | Analysis | | Platform | Sanger Sequencing | Comments | | Reference | Pang_et_al_2010 | Pubmed ID | 20482838 | Accession Number(s) | esv1007027
| Frequency | Sample Size | 3 | Observed Gain | 0 | Observed Loss | 0 | Observed Complex | 0 | Frequency | n/a |
|
|