esv1791687
- 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: 94 SVs from 16 studies. See in: genome view
Overlapping variant regions from other studies: 94 SVs from 16 studies. See in: genome view
Overlapping variant regions from other studies: 21 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 |
|---|---|---|---|---|---|---|---|---|---|
| esv1791687 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000005.10 | Chr5 | 78,279,919 | 78,279,919 |
| esv1791687 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000005.9 | Chr5 | 77,575,743 | 77,575,743 |
| esv1791687 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000005.8 | Chr5 | 77,611,499 | 77,611,499 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| essv4334093 | Remapped | Perfect | NC_000005.10:g.782 79919_78279920insG ACTTAAATATATATATAT AT | GRCh38.p12 | First Pass | NC_000005.10 | Chr5 | 78,279,919 | 78,279,919 |
| essv4334093 | Remapped | Perfect | NC_000005.9:g.7757 5743_77575744insGA CTTAAATATATATATATA T | GRCh37.p13 | First Pass | NC_000005.9 | Chr5 | 77,575,743 | 77,575,743 |
| essv4334093 | Submitted genomic | NC_000005.8:g.7761 1499_77611500insGA CTTAAATATATATATATA T | NCBI36 (hg18) | NC_000005.8 | Chr5 | 77,611,499 | 77,611,499 |