esv1817748
- Organism: Homo sapiens
- Study:estd188 (Pinto et al. 2011)
- Variant Type:copy number variation
- Method Type:Oligo aCGH
- Submitted on:NCBI36 (hg18)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:152,266
- Publication(s):Pinto et al. 2011
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: 718 SVs from 67 studies. See in: genome view
Overlapping variant regions from other studies: 718 SVs from 67 studies. See in: genome view
Overlapping variant regions from other studies: 276 SVs from 20 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 |
|---|---|---|---|---|---|---|---|---|---|
| esv1817748 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000011.10 | Chr11 | 131,919,018 | 132,071,283 |
| esv1817748 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000011.9 | Chr11 | 131,788,912 | 131,941,177 |
| esv1817748 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000011.8 | Chr11 | 131,294,122 | 131,446,387 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| essv4372794 | Remapped | Perfect | NC_000011.10:g.(?_ 131919018)_(132071 283_?)del | GRCh38.p12 | First Pass | NC_000011.10 | Chr11 | 131,919,018 | 132,071,283 |
| essv4372794 | Remapped | Perfect | NC_000011.9:g.(?_1 31788912)_(1319411 77_?)del | GRCh37.p13 | First Pass | NC_000011.9 | Chr11 | 131,788,912 | 131,941,177 |
| essv4372794 | Submitted genomic | NC_000011.8:g.(?_1 31294122)_(1314463 87_?)del | NCBI36 (hg18) | NC_000011.8 | Chr11 | 131,294,122 | 131,446,387 |