esv22589
- Organism: Homo sapiens
- Study:estd20 (Conrad et al. 2009)
- Variant Type:sequence alteration
- Method Type:Oligo aCGH
- Submitted on:NCBI36 (hg18)
- Variant Calls:3
- Validation:Not tested
- Clinical Assertions: No
- Region Size:80,857
- 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: 638 SVs from 77 studies. See in: genome view
Overlapping variant regions from other studies: 638 SVs from 77 studies. See in: genome view
Overlapping variant regions from other studies: 235 SVs from 25 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 |
|---|---|---|---|---|---|---|---|---|---|
| esv22589 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000001.11 | Chr1 | 189,736,108 | 189,816,964 |
| esv22589 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000001.10 | Chr1 | 189,705,238 | 189,786,094 |
| esv22589 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000001.9 | Chr1 | 187,971,861 | 188,052,717 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|
| esv17561 | Remapped | Perfect | GRCh38.p12 | First Pass | NC_000001.11 | Chr1 | 189,736,108 | 189,811,339 |
| esv15213 | Remapped | Perfect | GRCh38.p12 | First Pass | NC_000001.11 | Chr1 | 189,803,000 | 189,808,579 |
| esv21130 | Remapped | Perfect | GRCh38.p12 | First Pass | NC_000001.11 | Chr1 | 189,808,261 | 189,816,964 |
| esv17561 | Remapped | Perfect | GRCh37.p13 | First Pass | NC_000001.10 | Chr1 | 189,705,238 | 189,780,469 |
| esv15213 | Remapped | Perfect | GRCh37.p13 | First Pass | NC_000001.10 | Chr1 | 189,772,130 | 189,777,709 |
| esv21130 | Remapped | Perfect | GRCh37.p13 | First Pass | NC_000001.10 | Chr1 | 189,777,391 | 189,786,094 |
| esv17561 | Submitted genomic | NCBI36 (hg18) | NC_000001.9 | Chr1 | 187,971,861 | 188,047,092 | ||
| esv15213 | Submitted genomic | NCBI36 (hg18) | NC_000001.9 | Chr1 | 188,038,753 | 188,044,332 | ||
| esv21130 | Submitted genomic | NCBI36 (hg18) | NC_000001.9 | Chr1 | 188,044,014 | 188,052,717 |