esv3310547
- Organism: Homo sapiens
- Study:estd59 (1000 Genomes Consortium Pilot Project)
- Variant Type:novel sequence insertion
- Method Type:Sequencing
- Submitted on:NCBI36 (hg18)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:1,039
- Publication(s):1000 Genomes Project Consortium et al. 2010
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: 263 SVs from 44 studies. See in: genome view
Overlapping variant regions from other studies: 263 SVs from 44 studies. See in: genome view
Overlapping variant regions from other studies: 170 SVs from 13 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Outer Start | Inner Start | Inner Stop | Outer Stop |
|---|---|---|---|---|---|---|---|---|---|---|---|
| esv3310547 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000011.10 | Chr11 | 133,353,823 | 133,354,861 | 133,353,823 | 133,354,861 |
| esv3310547 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000011.9 | Chr11 | 133,223,718 | 133,224,756 | 133,223,718 | 133,224,756 |
| esv3310547 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000011.8 | Chr11 | 132,728,928 | 132,729,966 | 132,728,928 | 132,729,966 |
Variant Call Information
| Variant Call ID | Type | Sample ID | Method | Analysis | Other Calls in this Sample and Study |
|---|---|---|---|---|---|
| essv7843520 | novel sequence insertion | SAMN00001696 | Sequencing | Paired-end mapping | 44,056 |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Outer Start | Inner Start | Inner Stop | Outer Stop |
|---|---|---|---|---|---|---|---|---|---|---|---|
| essv7843520 | Remapped | Perfect | NC_000011.10:g.(13 3353823_133354861) _(133353823_133354 861)ins1525 | GRCh38.p12 | First Pass | NC_000011.10 | Chr11 | 133,353,823 | 133,354,861 | 133,353,823 | 133,354,861 |
| essv7843520 | Remapped | Perfect | NC_000011.9:g.(133 223718_133224756)_ (133223718_1332247 56)ins1525 | GRCh37.p13 | First Pass | NC_000011.9 | Chr11 | 133,223,718 | 133,224,756 | 133,223,718 | 133,224,756 |
| essv7843520 | Submitted genomic | NC_000011.8:g.(132 728928_132729966)_ (132728928_1327299 66)ins1525 | NCBI36 (hg18) | NC_000011.8 | Chr11 | 132,728,928 | 132,729,966 | 132,728,928 | 132,729,966 |