esv1791663
- 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: 108 SVs from 22 studies. See in: genome view
Overlapping variant regions from other studies: 108 SVs from 22 studies. See in: genome view
Overlapping variant regions from other studies: 23 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 |
|---|---|---|---|---|---|---|---|---|---|
| esv1791663 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000010.11 | Chr10 | 95,288,565 | 95,288,565 |
| esv1791663 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000010.10 | Chr10 | 97,048,322 | 97,048,322 |
| esv1791663 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000010.9 | Chr10 | 97,038,312 | 97,038,312 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| essv3698881 | Remapped | Perfect | NC_000010.11:g.952 88565_95288566insT | GRCh38.p12 | First Pass | NC_000010.11 | Chr10 | 95,288,565 | 95,288,565 |
| essv3698881 | Remapped | Perfect | NC_000010.10:g.970 48322_97048323insT | GRCh37.p13 | First Pass | NC_000010.10 | Chr10 | 97,048,322 | 97,048,322 |
| essv3698881 | Submitted genomic | NC_000010.9:g.9703 8312_97038313insT | NCBI36 (hg18) | NC_000010.9 | Chr10 | 97,038,312 | 97,038,312 |