esv1987260
- 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: 83 SVs from 26 studies. See in: genome view
Overlapping variant regions from other studies: 83 SVs from 26 studies. See in: genome view
Overlapping variant regions from other studies: 22 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 |
|---|---|---|---|---|---|---|---|---|---|
| esv1987260 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000012.12 | Chr12 | 111,361,721 | 111,361,721 |
| esv1987260 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000012.11 | Chr12 | 111,799,525 | 111,799,525 |
| esv1987260 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000012.10 | Chr12 | 110,283,908 | 110,283,908 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| essv4909356 | Remapped | Perfect | NC_000012.12:g.111 361721_111361722in sTGT | GRCh38.p12 | First Pass | NC_000012.12 | Chr12 | 111,361,721 | 111,361,721 |
| essv4909356 | Remapped | Perfect | NC_000012.11:g.111 799525_111799526in sTGT | GRCh37.p13 | First Pass | NC_000012.11 | Chr12 | 111,799,525 | 111,799,525 |
| essv4909356 | Submitted genomic | NC_000012.10:g.110 283908_110283909in sTGT | NCBI36 (hg18) | NC_000012.10 | Chr12 | 110,283,908 | 110,283,908 |