esv1003885
- 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:22,245
- 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: 466 SVs from 73 studies. See in: genome view
Overlapping variant regions from other studies: 466 SVs from 73 studies. See in: genome view
Overlapping variant regions from other studies: 228 SVs from 23 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 |
|---|---|---|---|---|---|---|---|---|---|
| esv1003885 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000012.12 | Chr12 | 131,245,782 | 131,268,026 |
| esv1003885 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000012.11 | Chr12 | 131,730,327 | 131,752,571 |
| esv1003885 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000012.10 | Chr12 | 130,296,280 | 130,318,524 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| essv3586474 | Remapped | Perfect | NC_000012.12:g.(?_ 131245782)_(131268 026_?)del | GRCh38.p12 | First Pass | NC_000012.12 | Chr12 | 131,245,782 | 131,268,026 |
| essv3586474 | Remapped | Perfect | NC_000012.11:g.(?_ 131730327)_(131752 571_?)del | GRCh37.p13 | First Pass | NC_000012.11 | Chr12 | 131,730,327 | 131,752,571 |
| essv3586474 | Submitted genomic | NC_000012.10:g.(?_ 130296280)_(130318 524_?)del | NCBI36 (hg18) | NC_000012.10 | Chr12 | 130,296,280 | 130,318,524 |