esv1711460
- Organism: Homo sapiens
- Study:estd22 (Levy et al. 2007)
- Variant Type:copy number variation
- Method Type:Sequencing
- Submitted on:NCBI36 (hg18)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:5,634
- Publication(s):Levy et al. 2007
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: 168 SVs from 41 studies. See in: genome view
Overlapping variant regions from other studies: 168 SVs from 41 studies. See in: genome view
Overlapping variant regions from other studies: 30 SVs from 13 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| esv1711460 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000011.10 | Chr11 | 94,234,821 | 94,240,454 |
| esv1711460 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000011.9 | Chr11 | 93,967,987 | 93,973,620 |
| esv1711460 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000011.8 | Chr11 | 93,607,635 | 93,613,268 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| essv4191911 | Remapped | Perfect | NC_000011.10:g.942 34821_94240454del | GRCh38.p12 | First Pass | NC_000011.10 | Chr11 | 94,234,821 | 94,240,454 |
| essv4191911 | Remapped | Perfect | NC_000011.9:g.9396 7987_93973620del | GRCh37.p13 | First Pass | NC_000011.9 | Chr11 | 93,967,987 | 93,973,620 |
| essv4191911 | Submitted genomic | NC_000011.8:g.9360 7635_93613268del | NCBI36 (hg18) | NC_000011.8 | Chr11 | 93,607,635 | 93,613,268 |