nsv436822
- Organism: Homo sapiens
- Study:nstd16 (Korbel et al. 2007)
- Variant Type:insertion
- Method Type:Sequencing
- Submitted on:NCBI36 (hg18)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:15,123
- Description:Unmated-Insertion
- Publication(s):Korbel et al. 2007
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: 843 SVs from 89 studies. See in: genome view
Overlapping variant regions from other studies: 843 SVs from 89 studies. See in: genome view
Overlapping variant regions from other studies: 399 SVs from 28 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Outer Start | Outer Stop |
|---|---|---|---|---|---|---|---|---|---|
| nsv436822 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000011.10 | Chr11 | 18,926,637 | 18,941,759 |
| nsv436822 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000011.9 | Chr11 | 18,948,184 | 18,963,306 |
| nsv436822 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000011.8 | Chr11 | 18,904,760 | 18,919,882 |
Variant Call Information
| Variant Call ID | Type | Sample ID | Method | Analysis | Other Calls in this Sample and Study |
|---|---|---|---|---|---|
| nssv466643 | insertion | SAMN00001583 | Sequencing | Paired-end mapping | 822 |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Outer Start | Outer Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv466643 | Remapped | Perfect | NC_000011.10:g.(18 926637_?)_(?_18941 759)ins? | GRCh38.p12 | First Pass | NC_000011.10 | Chr11 | 18,926,637 | 18,941,759 |
| nssv466643 | Remapped | Perfect | NC_000011.9:g.(189 48184_?)_(?_189633 06)ins? | GRCh37.p13 | First Pass | NC_000011.9 | Chr11 | 18,948,184 | 18,963,306 |
| nssv466643 | Submitted genomic | NC_000011.8:g.(189 04760_?)_(?_189198 82)ins(0_?) | NCBI36 (hg18) | NC_000011.8 | Chr11 | 18,904,760 | 18,919,882 |