esv1301506
- 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:6,110
- 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: 154 SVs from 54 studies. See in: genome view
Overlapping variant regions from other studies: 154 SVs from 54 studies. See in: genome view
Overlapping variant regions from other studies: 49 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 | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| esv1301506 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000005.10 | Chr5 | 58,384,174 | 58,390,283 |
| esv1301506 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000005.9 | Chr5 | 57,680,001 | 57,686,110 |
| esv1301506 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000005.8 | Chr5 | 57,715,758 | 57,721,867 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| essv3773463 | Remapped | Perfect | NC_000005.10:g.583 84174_58390283del | GRCh38.p12 | First Pass | NC_000005.10 | Chr5 | 58,384,174 | 58,390,283 |
| essv3773463 | Remapped | Perfect | NC_000005.9:g.5768 0001_57686110del | GRCh37.p13 | First Pass | NC_000005.9 | Chr5 | 57,680,001 | 57,686,110 |
| essv3773463 | Submitted genomic | NC_000005.8:g.5771 5758_57721867del | NCBI36 (hg18) | NC_000005.8 | Chr5 | 57,715,758 | 57,721,867 |