esv999186
- Organism: Homo sapiens
- Study:estd180 (Pang et al. 2010)
- Variant Type:insertion
- Method Type:Sequencing
- Submitted on:NCBI36 (hg18)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:14,532
- 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: 194 SVs from 45 studies. See in: genome view
Overlapping variant regions from other studies: 194 SVs from 45 studies. See in: genome view
Overlapping variant regions from other studies: 60 SVs from 14 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 |
|---|---|---|---|---|---|---|---|---|---|
| esv999186 | Remapped | Good | GRCh38.p12 | Primary Assembly | First Pass | NC_000003.12 | Chr3 | 68,017,838 | 68,032,369 |
| esv999186 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000003.11 | Chr3 | 68,066,982 | 68,081,519 |
| esv999186 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000003.10 | Chr3 | 68,149,672 | 68,164,209 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Outer Start | Outer Stop |
|---|---|---|---|---|---|---|---|---|---|
| essv3563517 | Remapped | Good | NC_000003.12:g.(68 017838_?)_(?_68032 369)ins9424 | GRCh38.p12 | First Pass | NC_000003.12 | Chr3 | 68,017,838 | 68,032,369 |
| essv3563517 | Remapped | Perfect | NC_000003.11:g.(68 066982_?)_(?_68081 519)ins9424 | GRCh37.p13 | First Pass | NC_000003.11 | Chr3 | 68,066,982 | 68,081,519 |
| essv3563517 | Submitted genomic | NC_000003.10:g.(68 149672_?)_(?_68164 209)ins9424 | NCBI36 (hg18) | NC_000003.10 | Chr3 | 68,149,672 | 68,164,209 |