esv1001126
- 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:24,874
- 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: 255 SVs from 64 studies. See in: genome view
Overlapping variant regions from other studies: 263 SVs from 64 studies. See in: genome view
Overlapping variant regions from other studies: 111 SVs from 22 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 |
|---|---|---|---|---|---|---|---|---|---|
| esv1001126 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000007.14 | Chr7 | 64,359,058 | 64,383,931 |
| esv1001126 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000007.13 | Chr7 | 63,819,436 | 63,844,309 |
| esv1001126 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000007.12 | Chr7 | 63,456,871 | 63,481,744 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| essv3586600 | Remapped | Perfect | NC_000007.14:g.(?_ 64359058)_(6438393 1_?)dup | GRCh38.p12 | First Pass | NC_000007.14 | Chr7 | 64,359,058 | 64,383,931 |
| essv3586600 | Remapped | Perfect | NC_000007.13:g.(?_ 63819436)_(6384430 9_?)dup | GRCh37.p13 | First Pass | NC_000007.13 | Chr7 | 63,819,436 | 63,844,309 |
| essv3586600 | Submitted genomic | NC_000007.12:g.(?_ 63456871)_(6348174 4_?)dup | NCBI36 (hg18) | NC_000007.12 | Chr7 | 63,456,871 | 63,481,744 |