esv2234632
- Organism: Homo sapiens
- Study:estd194 (Bentley et al. 2008)
- Variant Type:copy number variation
- Method Type:Sequencing
- Submitted on:NCBI36 (hg18)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:2
- Publication(s):Bentley et al. 2008
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: 125 SVs from 26 studies. See in: genome view
Overlapping variant regions from other studies: 125 SVs from 26 studies. See in: genome view
Overlapping variant regions from other studies: 35 SVs from 9 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| esv2234632 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000003.12 | Chr3 | 119,150,336 | 119,150,337 |
| esv2234632 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000003.11 | Chr3 | 118,869,183 | 118,869,184 |
| esv2234632 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000003.10 | Chr3 | 120,351,873 | 120,351,874 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| essv4954990 | Remapped | Perfect | NC_000003.12:g.119 150336_119150337de lA | GRCh38.p12 | First Pass | NC_000003.12 | Chr3 | 119,150,336 | 119,150,337 |
| essv4954990 | Remapped | Perfect | NC_000003.11:g.118 869183_118869184de lA | GRCh37.p13 | First Pass | NC_000003.11 | Chr3 | 118,869,183 | 118,869,184 |
| essv4954990 | Submitted genomic | NC_000003.10:g.120 351873_120351874de lA | NCBI36 (hg18) | NC_000003.10 | Chr3 | 120,351,873 | 120,351,874 |