nsv513731
- 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:8,732
- 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: 161 SVs from 30 studies. See in: genome view
Overlapping variant regions from other studies: 161 SVs from 30 studies. See in: genome view
Overlapping variant regions from other studies: 46 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 | Outer Start | Outer Stop |
|---|---|---|---|---|---|---|---|---|---|
| nsv513731 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000002.12 | Chr2 | 150,196,615 | 150,205,346 |
| nsv513731 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000002.11 | Chr2 | 151,053,129 | 151,061,860 |
| nsv513731 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000002.10 | Chr2 | 150,761,375 | 150,770,106 |
Variant Call Information
| Variant Call ID | Type | Sample ID | Method | Analysis | Other Calls in this Sample and Study |
|---|---|---|---|---|---|
| nssv626983 | 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 |
|---|---|---|---|---|---|---|---|---|---|
| nssv626983 | Remapped | Perfect | NC_000002.12:g.(15 0196615_?)_(?_1502 05346)ins8732 | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 150,196,615 | 150,205,346 |
| nssv626983 | Remapped | Perfect | NC_000002.11:g.(15 1053129_?)_(?_1510 61860)ins8732 | GRCh37.p13 | First Pass | NC_000002.11 | Chr2 | 151,053,129 | 151,061,860 |
| nssv626983 | Submitted genomic | NC_000002.10:g.(15 0761375_?)_(?_1507 70106)ins8732 | NCBI36 (hg18) | NC_000002.10 | Chr2 | 150,761,375 | 150,770,106 |