esv1097647
- Organism: Homo sapiens
- Study:estd22 (Levy et al. 2007)
- Variant Type:copy number variation
- Method Type:Sequencing
- Submitted on:NCBI36 (hg18)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:7,853
- Publication(s):Levy et al. 2007
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: 438 SVs from 69 studies. See in: genome view
Overlapping variant regions from other studies: 438 SVs from 69 studies. See in: genome view
Overlapping variant regions from other studies: 225 SVs from 23 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| esv1097647 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000007.14 | Chr7 | 154,600,191 | 154,608,043 |
| esv1097647 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000007.13 | Chr7 | 154,391,901 | 154,399,753 |
| esv1097647 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000007.12 | Chr7 | 154,022,834 | 154,030,686 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| essv3736763 | Remapped | Perfect | NC_000007.14:g.154 600191_154608043de l | GRCh38.p12 | First Pass | NC_000007.14 | Chr7 | 154,600,191 | 154,608,043 |
| essv3736763 | Remapped | Perfect | NC_000007.13:g.154 391901_154399753de l | GRCh37.p13 | First Pass | NC_000007.13 | Chr7 | 154,391,901 | 154,399,753 |
| essv3736763 | Submitted genomic | NC_000007.12:g.154 022834_154030686de l | NCBI36 (hg18) | NC_000007.12 | Chr7 | 154,022,834 | 154,030,686 |