esv1407091
- 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:3
- 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: 218 SVs from 20 studies. See in: genome view
Overlapping variant regions from other studies: 218 SVs from 20 studies. See in: genome view
Overlapping variant regions from other studies: 77 SVs from 10 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| esv1407091 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000018.10 | Chr18 | 50,971,941 | 50,971,943 |
| esv1407091 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000018.9 | Chr18 | 48,498,311 | 48,498,313 |
| esv1407091 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000018.8 | Chr18 | 46,752,309 | 46,752,311 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| essv3969119 | Remapped | Perfect | NC_000018.10:g.509 71941_50971943del | GRCh38.p12 | First Pass | NC_000018.10 | Chr18 | 50,971,941 | 50,971,943 |
| essv3969119 | Remapped | Perfect | NC_000018.9:g.4849 8311_48498313del | GRCh37.p13 | First Pass | NC_000018.9 | Chr18 | 48,498,311 | 48,498,313 |
| essv3969119 | Submitted genomic | NC_000018.8:g.4675 2309_46752311del | NCBI36 (hg18) | NC_000018.8 | Chr18 | 46,752,309 | 46,752,311 |