esv1802311
- 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:35,454
- 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: 229 SVs from 53 studies. See in: genome view
Overlapping variant regions from other studies: 229 SVs from 53 studies. See in: genome view
Overlapping variant regions from other studies: 72 SVs from 15 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 |
|---|---|---|---|---|---|---|---|---|---|
| esv1802311 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000007.14 | Chr7 | 129,767,096 | 129,802,549 |
| esv1802311 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000007.13 | Chr7 | 129,406,936 | 129,442,389 |
| esv1802311 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000007.12 | Chr7 | 129,194,172 | 129,229,625 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| essv4421899 | Remapped | Perfect | NC_000007.14:g.(?_ 129767096)_(129802 549_?)dup | GRCh38.p12 | First Pass | NC_000007.14 | Chr7 | 129,767,096 | 129,802,549 |
| essv4421899 | Remapped | Perfect | NC_000007.13:g.(?_ 129406936)_(129442 389_?)dup | GRCh37.p13 | First Pass | NC_000007.13 | Chr7 | 129,406,936 | 129,442,389 |
| essv4421899 | Submitted genomic | NC_000007.12:g.(?_ 129194172)_(129229 625_?)dup | NCBI36 (hg18) | NC_000007.12 | Chr7 | 129,194,172 | 129,229,625 |