esv2421295
- 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: 57 SVs from 13 studies. See in: genome view
Overlapping variant regions from other studies: 57 SVs from 13 studies. See in: genome view
Overlapping variant regions from other studies: 18 SVs from 8 studies. See in: genome view
Variant Region Placement Information
Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
---|---|---|---|---|---|---|---|---|---|
esv2421295 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000010.11 | Chr10 | 24,408,730 | 24,408,730 |
esv2421295 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000010.10 | Chr10 | 24,697,659 | 24,697,659 |
esv2421295 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000010.9 | Chr10 | 24,737,665 | 24,737,665 |
Variant Call Information
Variant Call Placement Information
Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
---|---|---|---|---|---|---|---|---|---|
essv4532335 | Remapped | Perfect | NC_000010.11:g.244 08730_24408731insT | GRCh38.p12 | First Pass | NC_000010.11 | Chr10 | 24,408,730 | 24,408,730 |
essv4532335 | Remapped | Perfect | NC_000010.10:g.246 97659_24697660insT | GRCh37.p13 | First Pass | NC_000010.10 | Chr10 | 24,697,659 | 24,697,659 |
essv4532335 | Submitted genomic | NC_000010.9:g.2473 7665_24737666insT | NCBI36 (hg18) | NC_000010.9 | Chr10 | 24,737,665 | 24,737,665 |