esv1708125
- Organism: Homo sapiens
- Study:estd22 (Levy et al. 2007)
- Variant Type:copy number variation
- Method Type:Sequencing
- Submitted on:NCBI36 (hg18)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:6,251
- Publication(s):Levy et al. 2007
Source: NCBI
- Genome View
- Variant Region Details and Evidence
- Validation Information
- Clinical Assertions
- Genotype Information
Genome View
Select assembly:Overlapping variant regions from other studies: 542 SVs from 50 studies. See in: genome view
Overlapping variant regions from other studies: 543 SVs from 50 studies. See in: genome view
Overlapping variant regions from other studies: 234 SVs from 12 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| esv1708125 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000023.11 | ChrX | 11,935,080 | 11,941,330 |
| esv1708125 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000023.10 | ChrX | 11,953,199 | 11,959,449 |
| esv1708125 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000023.9 | ChrX | 11,863,120 | 11,869,370 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| essv4218766 | Remapped | Perfect | NC_000023.11:g.119 35080_11941330del | GRCh38.p12 | First Pass | NC_000023.11 | ChrX | 11,935,080 | 11,941,330 |
| essv4218766 | Remapped | Perfect | NC_000023.10:g.119 53199_11959449del | GRCh37.p13 | First Pass | NC_000023.10 | ChrX | 11,953,199 | 11,959,449 |
| essv4218766 | Submitted genomic | NC_000023.9:g.1186 3120_11869370del | NCBI36 (hg18) | NC_000023.9 | ChrX | 11,863,120 | 11,869,370 |