esv992503
- 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:26,422
- 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: 294 SVs from 40 studies. See in: genome view
Overlapping variant regions from other studies: 308 SVs from 41 studies. See in: genome view
Overlapping variant regions from other studies: 117 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 | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| esv992503 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000001.11 | Chr1 | 586,078 | 612,499 |
| esv992503 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000001.10 | Chr1 | 521,458 | 547,879 |
| esv992503 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000001.9 | Chr1 | 511,321 | 537,742 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| essv3586722 | Remapped | Perfect | NC_000001.11:g.(?_ 586078)_(612499_?) del | GRCh38.p12 | First Pass | NC_000001.11 | Chr1 | 586,078 | 612,499 |
| essv3586722 | Remapped | Perfect | NC_000001.10:g.(?_ 521458)_(547879_?) del | GRCh37.p13 | First Pass | NC_000001.10 | Chr1 | 521,458 | 547,879 |
| essv3586722 | Submitted genomic | NC_000001.9:g.(?_5 11321)_(537742_?)d el | NCBI36 (hg18) | NC_000001.9 | Chr1 | 511,321 | 537,742 |