esv2421321
- 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: 279 SVs from 38 studies. See in: genome view
Overlapping variant regions from other studies: 126 SVs from 18 studies. See in: genome view
Overlapping variant regions from other studies: 279 SVs from 38 studies. See in: genome view
Overlapping variant regions from other studies: 143 SVs from 12 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| esv2421321 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000011.10 | Chr11 | 514,581 | 514,581 |
| esv2421321 | Remapped | Perfect | GRCh38.p12 | ALT_REF_LOCI_1 | Second Pass | NT_187586.1 | Chr11|NT_1 87586.1 | 44,222 | 44,222 |
| esv2421321 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000011.9 | Chr11 | 514,581 | 514,581 |
| esv2421321 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000011.8 | Chr11 | 504,581 | 504,581 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| essv4501316 | Remapped | Perfect | NT_187586.1:g.4422 2_44223insTAT | GRCh38.p12 | Second Pass | NT_187586.1 | Chr11|NT_1 87586.1 | 44,222 | 44,222 |
| essv4501316 | Remapped | Perfect | NC_000011.10:g.514 581_514582insTAT | GRCh38.p12 | First Pass | NC_000011.10 | Chr11 | 514,581 | 514,581 |
| essv4501316 | Remapped | Perfect | NC_000011.9:g.5145 81_514582insTAT | GRCh37.p13 | First Pass | NC_000011.9 | Chr11 | 514,581 | 514,581 |
| essv4501316 | Submitted genomic | NC_000011.8:g.5045 81_504582insTAT | NCBI36 (hg18) | NC_000011.8 | Chr11 | 504,581 | 504,581 |