esv11445
- Organism: Homo sapiens
- Study:estd20 (Conrad et al. 2009)
- Variant Type:copy number variation
- Method Type:Oligo aCGH
- Submitted on:NCBI36 (hg18)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:57,246
- Publication(s):Conrad et al. 2009
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: 537 SVs from 40 studies. See in: genome view
Overlapping variant regions from other studies: 537 SVs from 40 studies. See in: genome view
Overlapping variant regions from other studies: 228 SVs from 11 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| esv11445 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000023.11 | ChrX | 126,099,415 | 126,156,660 |
| esv11445 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000023.10 | ChrX | 125,233,398 | 125,290,643 |
| esv11445 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000023.9 | ChrX | 125,061,079 | 125,118,324 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| essv77244 | Remapped | Perfect | NC_000023.11:g.(?_ 126099415)_(126156 660_?)del | GRCh38.p12 | First Pass | NC_000023.11 | ChrX | 126,099,415 | 126,156,660 |
| essv77244 | Remapped | Perfect | NC_000023.10:g.(?_ 125233398)_(125290 643_?)del | GRCh37.p13 | First Pass | NC_000023.10 | ChrX | 125,233,398 | 125,290,643 |
| essv77244 | Submitted genomic | NC_000023.9:g.(?_1 25061079)_(1251183 24_?)del | NCBI36 (hg18) | NC_000023.9 | ChrX | 125,061,079 | 125,118,324 |