nsv513314
- Organism: Homo sapiens
- Study:nstd50 (Arlt et al. 2011)
- Variant Type:insertion
- Method Type:Sequencing
- Submitted on:NCBI36 (hg18)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:1,807
- Publication(s):Arlt et al. 2011
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: 131 SVs from 35 studies. See in: genome view
Overlapping variant regions from other studies: 131 SVs from 35 studies. See in: genome view
Overlapping variant regions from other studies: 43 SVs from 11 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv513314 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000011.10 | Chr11 | 45,100,632 | 45,102,438 |
| nsv513314 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000011.9 | Chr11 | 45,122,183 | 45,123,989 |
| nsv513314 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000011.8 | Chr11 | 45,078,759 | 45,080,565 |
Variant Call Information
| Variant Call ID | Type | Sample ID | Method | Analysis | Other Calls in this Sample and Study |
|---|---|---|---|---|---|
| nssv625701 | insertion | 1 | Sequencing | Paired-end mapping | 2,637 |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Outer Start | Outer Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv625701 | Remapped | Perfect | NC_000011.10:g.(45 100632_?)_(?_45102 438)ins781 | GRCh38.p12 | First Pass | NC_000011.10 | Chr11 | 45,100,632 | 45,102,438 |
| nssv625701 | Remapped | Perfect | NC_000011.9:g.(451 22183_?)_(?_451239 89)ins781 | GRCh37.p13 | First Pass | NC_000011.9 | Chr11 | 45,122,183 | 45,123,989 |
| nssv625701 | Submitted genomic | NC_000011.8:g.(450 78759_?)_(?_450805 65)ins781 | NCBI36 (hg18) | NC_000011.8 | Chr11 | 45,078,759 | 45,080,565 |