esv992392
- Organism: Homo sapiens
- Study:estd180 (Pang et al. 2010)
- Variant Type:copy number variation
- Method Type:Oligo aCGH
- Submitted on:NCBI36 (hg18)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:20,458
- Publication(s):Pang et al. 2010
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: 1515 SVs from 92 studies. See in: genome view
Overlapping variant regions from other studies: 1515 SVs from 92 studies. See in: genome view
Overlapping variant regions from other studies: 702 SVs from 30 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 |
|---|---|---|---|---|---|---|---|---|---|
| esv992392 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000015.10 | Chr15 | 24,240,911 | 24,261,368 |
| esv992392 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000015.9 | Chr15 | 24,486,058 | 24,506,515 |
| esv992392 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000015.8 | Chr15 | 22,037,151 | 22,057,608 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| essv3586660 | Remapped | Perfect | NC_000015.10:g.(?_ 24240911)_(2426136 8_?)dup | GRCh38.p12 | First Pass | NC_000015.10 | Chr15 | 24,240,911 | 24,261,368 |
| essv3586660 | Remapped | Perfect | NC_000015.9:g.(?_2 4486058)_(24506515 _?)dup | GRCh37.p13 | First Pass | NC_000015.9 | Chr15 | 24,486,058 | 24,506,515 |
| essv3586660 | Submitted genomic | NC_000015.8:g.(?_2 2037151)_(22057608 _?)dup | NCBI36 (hg18) | NC_000015.8 | Chr15 | 22,037,151 | 22,057,608 |