esv1791665
- 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: 178 SVs from 35 studies. See in: genome view
Overlapping variant regions from other studies: 178 SVs from 35 studies. See in: genome view
Overlapping variant regions from other studies: 51 SVs from 14 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| esv1791665 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000004.12 | Chr4 | 98,082,433 | 98,082,433 |
| esv1791665 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000004.11 | Chr4 | 99,003,584 | 99,003,584 |
| esv1791665 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000004.10 | Chr4 | 99,222,607 | 99,222,607 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| essv3788983 | Remapped | Perfect | NC_000004.12:g.980 82433_98082434insT T | GRCh38.p12 | First Pass | NC_000004.12 | Chr4 | 98,082,433 | 98,082,433 |
| essv3788983 | Remapped | Perfect | NC_000004.11:g.990 03584_99003585insT T | GRCh37.p13 | First Pass | NC_000004.11 | Chr4 | 99,003,584 | 99,003,584 |
| essv3788983 | Submitted genomic | NC_000004.10:g.992 22607_99222608insT T | NCBI36 (hg18) | NC_000004.10 | Chr4 | 99,222,607 | 99,222,607 |