esv993198
- 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:27,120
- 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: 152 SVs from 35 studies. See in: genome view
Overlapping variant regions from other studies: 155 SVs from 35 studies. See in: genome view
Overlapping variant regions from other studies: 59 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 | Outer Start | Outer Stop |
|---|---|---|---|---|---|---|---|---|---|
| esv993198 | Remapped | Pass | GRCh38.p12 | Primary Assembly | First Pass | NC_000002.12 | Chr2 | 18,999,825 | 19,026,944 |
| esv993198 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000002.11 | Chr2 | 19,181,098 | 19,226,699 |
| esv993198 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000002.10 | Chr2 | 19,044,579 | 19,090,180 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Outer Start | Outer Stop |
|---|---|---|---|---|---|---|---|---|---|
| essv3565686 | Remapped | Pass | NC_000002.12:g.(18 999825_?)_(?_19026 944)del | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 18,999,825 | 19,026,944 |
| essv3565686 | Remapped | Perfect | NC_000002.11:g.(19 181098_?)_(?_19226 699)del | GRCh37.p13 | First Pass | NC_000002.11 | Chr2 | 19,181,098 | 19,226,699 |
| essv3565686 | Submitted genomic | NC_000002.10:g.(19 044579_?)_(?_19090 180)del21178 | NCBI36 (hg18) | NC_000002.10 | Chr2 | 19,044,579 | 19,090,180 |