esv1628398
- Organism: Homo sapiens
- Study:estd22 (Levy et al. 2007)
- Variant Type:inversion
- Method Type:Sequencing
- Submitted on:NCBI36 (hg18)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:1,539
- 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: 220 SVs from 57 studies. See in: genome view
Overlapping variant regions from other studies: 221 SVs from 57 studies. See in: genome view
Overlapping variant regions from other studies: 84 SVs from 19 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| esv1628398 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000012.12 | Chr12 | 12,392,045 | 12,393,583 |
| esv1628398 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000012.11 | Chr12 | 12,544,979 | 12,546,517 |
| esv1628398 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000012.10 | Chr12 | 12,436,246 | 12,437,784 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| essv3776758 | Remapped | Perfect | NC_000012.12:g.123 92045_12393583inv | GRCh38.p12 | First Pass | NC_000012.12 | Chr12 | 12,392,045 | 12,393,583 |
| essv3776758 | Remapped | Perfect | NC_000012.11:g.125 44979_12546517inv | GRCh37.p13 | First Pass | NC_000012.11 | Chr12 | 12,544,979 | 12,546,517 |
| essv3776758 | Submitted genomic | NC_000012.10:g.124 36246_12437784inv | NCBI36 (hg18) | NC_000012.10 | Chr12 | 12,436,246 | 12,437,784 |