esv1791680
- 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: 148 SVs from 21 studies. See in: genome view
Overlapping variant regions from other studies: 148 SVs from 21 studies. See in: genome view
Overlapping variant regions from other studies: 58 SVs from 11 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| esv1791680 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000005.10 | Chr5 | 88,956,297 | 88,956,297 |
| esv1791680 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000005.9 | Chr5 | 88,252,114 | 88,252,114 |
| esv1791680 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000005.8 | Chr5 | 88,287,870 | 88,287,870 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| essv4007998 | Remapped | Perfect | NC_000005.10:g.889 56297_88956298insA | GRCh38.p12 | First Pass | NC_000005.10 | Chr5 | 88,956,297 | 88,956,297 |
| essv4007998 | Remapped | Perfect | NC_000005.9:g.8825 2114_88252115insA | GRCh37.p13 | First Pass | NC_000005.9 | Chr5 | 88,252,114 | 88,252,114 |
| essv4007998 | Submitted genomic | NC_000005.8:g.8828 7870_88287871insA | NCBI36 (hg18) | NC_000005.8 | Chr5 | 88,287,870 | 88,287,870 |