nsv513435
- 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:1,769
- 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: 196 SVs from 42 studies. See in: genome view
Overlapping variant regions from other studies: 198 SVs from 42 studies. See in: genome view
Overlapping variant regions from other studies: 63 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv513435 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000015.10 | Chr15 | 83,694,195 | 83,695,963 |
| nsv513435 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000015.9 | Chr15 | 84,362,947 | 84,364,715 |
| nsv513435 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000015.8 | Chr15 | 82,153,951 | 82,155,719 |
Variant Call Information
| Variant Call ID | Type | Sample ID | Method | Analysis | Other Calls in this Sample and Study |
|---|---|---|---|---|---|
| nssv625836 | 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 |
|---|---|---|---|---|---|---|---|---|---|
| nssv625836 | Remapped | Perfect | NC_000015.10:g.(83 694195_?)_(?_83695 963)ins713 | GRCh38.p12 | First Pass | NC_000015.10 | Chr15 | 83,694,195 | 83,695,963 |
| nssv625836 | Remapped | Perfect | NC_000015.9:g.(843 62947_?)_(?_843647 15)ins713 | GRCh37.p13 | First Pass | NC_000015.9 | Chr15 | 84,362,947 | 84,364,715 |
| nssv625836 | Submitted genomic | NC_000015.8:g.(821 53951_?)_(?_821557 19)ins713 | NCBI36 (hg18) | NC_000015.8 | Chr15 | 82,153,951 | 82,155,719 |