esv1001413
- 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:55
- 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: 316 SVs from 36 studies. See in: genome view
Overlapping variant regions from other studies: 316 SVs from 36 studies. See in: genome view
Overlapping variant regions from other studies: 148 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 |
|---|---|---|---|---|---|---|---|---|---|
| esv1001413 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000018.10 | Chr18 | 11,014,274 | 11,014,328 |
| esv1001413 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000018.9 | Chr18 | 11,014,272 | 11,014,326 |
| esv1001413 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000018.8 | Chr18 | 11,004,272 | 11,004,326 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| essv3586000 | Remapped | Perfect | NC_000018.10:g.110 14274_11014328del5 5 | GRCh38.p12 | First Pass | NC_000018.10 | Chr18 | 11,014,274 | 11,014,328 |
| essv3586000 | Remapped | Perfect | NC_000018.9:g.1101 4272_11014326del55 | GRCh37.p13 | First Pass | NC_000018.9 | Chr18 | 11,014,272 | 11,014,326 |
| essv3586000 | Submitted genomic | NC_000018.8:g.1100 4272_11004326del55 | NCBI36 (hg18) | NC_000018.8 | Chr18 | 11,004,272 | 11,004,326 |