esv2421302
- 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: 91 SVs from 16 studies. See in: genome view
Overlapping variant regions from other studies: 91 SVs from 16 studies. See in: genome view
Overlapping variant regions from other studies: 46 SVs from 9 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| esv2421302 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000002.12 | Chr2 | 10,321,416 | 10,321,416 |
| esv2421302 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000002.11 | Chr2 | 10,461,542 | 10,461,542 |
| esv2421302 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000002.10 | Chr2 | 10,378,993 | 10,378,993 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| essv4991727 | Remapped | Perfect | NC_000002.12:g.103 21416_10321417insT | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 10,321,416 | 10,321,416 |
| essv4991727 | Remapped | Perfect | NC_000002.11:g.104 61542_10461543insT | GRCh37.p13 | First Pass | NC_000002.11 | Chr2 | 10,461,542 | 10,461,542 |
| essv4991727 | Submitted genomic | NC_000002.10:g.103 78993_10378994insT | NCBI36 (hg18) | NC_000002.10 | Chr2 | 10,378,993 | 10,378,993 |