esv1791709
- Organism: Homo sapiens
- Study:estd22 (Levy et al. 2007)
- Variant Type:insertion
- Method Type:Sequencing
- Submitted on:NCBI36 (hg18)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:1
- 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: 141 SVs from 21 studies. See in: genome view
Overlapping variant regions from other studies: 141 SVs from 21 studies. See in: genome view
Overlapping variant regions from other studies: 33 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 |
|---|---|---|---|---|---|---|---|---|---|
| esv1791709 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000002.12 | Chr2 | 136,872,838 | 136,872,838 |
| esv1791709 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000002.11 | Chr2 | 137,630,408 | 137,630,408 |
| esv1791709 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000002.10 | Chr2 | 137,346,878 | 137,346,878 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| essv4296878 | Remapped | Perfect | NC_000002.12:g.136 872838_136872839in sA | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 136,872,838 | 136,872,838 |
| essv4296878 | Remapped | Perfect | NC_000002.11:g.137 630408_137630409in sA | GRCh37.p13 | First Pass | NC_000002.11 | Chr2 | 137,630,408 | 137,630,408 |
| essv4296878 | Submitted genomic | NC_000002.10:g.137 346878_137346879in sA | NCBI36 (hg18) | NC_000002.10 | Chr2 | 137,346,878 | 137,346,878 |