esv989936
- Organism: Homo sapiens
- Study:estd180 (Pang et al. 2010)
- Variant Type:copy number variation
- Method Type:Sequencing
- Submitted on:NCBI36 (hg18)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:20,432
- 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: 553 SVs from 64 studies. See in: genome view
Overlapping variant regions from other studies: 553 SVs from 64 studies. See in: genome view
Overlapping variant regions from other studies: 371 SVs from 24 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Outer Start | Outer Stop |
|---|---|---|---|---|---|---|---|---|---|
| esv989936 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000002.12 | Chr2 | 179,196,464 | 179,216,895 |
| esv989936 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000002.11 | Chr2 | 180,061,191 | 180,081,622 |
| esv989936 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000002.10 | Chr2 | 179,769,436 | 179,789,867 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Outer Start | Outer Stop |
|---|---|---|---|---|---|---|---|---|---|
| essv3565250 | Remapped | Perfect | NC_000002.12:g.(17 9196464_?)_(?_1792 16895)del | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 179,196,464 | 179,216,895 |
| essv3565250 | Remapped | Perfect | NC_000002.11:g.(18 0061191_?)_(?_1800 81622)del | GRCh37.p13 | First Pass | NC_000002.11 | Chr2 | 180,061,191 | 180,081,622 |
| essv3565250 | Submitted genomic | NC_000002.10:g.(17 9769436_?)_(?_1797 89867)del15782 | NCBI36 (hg18) | NC_000002.10 | Chr2 | 179,769,436 | 179,789,867 |