esv2421309
- Organism: Homo sapiens
- Study:estd194 (Bentley et al. 2008)
- Variant Type:insertion
- Method Type:Sequencing
- Submitted on:NCBI36 (hg18)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:1
- Publication(s):Bentley et al. 2008
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: 144 SVs from 28 studies. See in: genome view
Overlapping variant regions from other studies: 144 SVs from 28 studies. See in: genome view
Overlapping variant regions from other studies: 56 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 |
|---|---|---|---|---|---|---|---|---|---|
| esv2421309 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000007.14 | Chr7 | 14,647,630 | 14,647,630 |
| esv2421309 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000007.13 | Chr7 | 14,687,255 | 14,687,255 |
| esv2421309 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000007.12 | Chr7 | 14,653,780 | 14,653,780 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| essv4896926 | Remapped | Perfect | NC_000007.14:g.146 47630_14647631insC | GRCh38.p12 | First Pass | NC_000007.14 | Chr7 | 14,647,630 | 14,647,630 |
| essv4896926 | Remapped | Perfect | NC_000007.13:g.146 87255_14687256insC | GRCh37.p13 | First Pass | NC_000007.13 | Chr7 | 14,687,255 | 14,687,255 |
| essv4896926 | Submitted genomic | NC_000007.12:g.146 53780_14653781insC | NCBI36 (hg18) | NC_000007.12 | Chr7 | 14,653,780 | 14,653,780 |