esv1000434
- 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:42,667
- 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: 598 SVs from 52 studies. See in: genome view
Overlapping variant regions from other studies: 598 SVs from 52 studies. See in: genome view
Overlapping variant regions from other studies: 301 SVs from 17 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 |
|---|---|---|---|---|---|---|---|---|---|
| esv1000434 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000018.10 | Chr18 | 74,422,735 | 74,465,401 |
| esv1000434 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000018.9 | Chr18 | 72,089,970 | 72,132,636 |
| esv1000434 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000018.8 | Chr18 | 70,240,950 | 70,283,616 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Outer Start | Outer Stop |
|---|---|---|---|---|---|---|---|---|---|
| essv3564404 | Remapped | Perfect | NC_000018.10:g.(74 422735_?)_(?_74465 401)del | GRCh38.p12 | First Pass | NC_000018.10 | Chr18 | 74,422,735 | 74,465,401 |
| essv3564404 | Remapped | Perfect | NC_000018.9:g.(720 89970_?)_(?_721326 36)del | GRCh37.p13 | First Pass | NC_000018.9 | Chr18 | 72,089,970 | 72,132,636 |
| essv3564404 | Submitted genomic | NC_000018.8:g.(702 40950_?)_(?_702836 16)del8978 | NCBI36 (hg18) | NC_000018.8 | Chr18 | 70,240,950 | 70,283,616 |