nsv481632
- Organism: Homo sapiens
- Study:nstd35 (Kidd et al. 2010)
- Variant Type:novel sequence insertion
- Method Type:Sequencing
- Variant is Defined by:GU269138
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:916
- Description:This variant by definition has no placement. It represents a contig assembled from multiple read pairs, no part of which could be mapped to assembly NCBI35.
- Publication(s):Kidd et al. 2010
Source: NCBI
- Genome View
- Variant Region Details and Evidence
- Validation Information
- Clinical Assertions
- Genotype Information
Genome View
Select assembly:
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|
| nsv481632 | Remapped | Pass | GRCh38.p12 | Primary Assembly | NT_187318.1 | Chr21|NT_1 87318.1 | 67,108 | 68,023 |
| nsv481632 | Remapped | Pass | GRCh38.p12 | Primary Assembly | NT_187317.1 | Chr21|NT_1 87317.1 | 95,195 | 96,110 |
| nsv481632 | Remapped | Pass | GRCh38.p12 | Primary Assembly | NT_187388.1 | Chr22|NT_1 87388.1 | 111,272 | 112,186 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis |
|---|---|---|---|
| nssv3019455 | novel sequence insertion | Sequencing | One end anchored assembly |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|
| nssv3019455 | Remapped | Pass | NT_187317.1:g.9519 5_96110ins?NT_1873 18.1:g.67108_68023 ins?NT_187388.1:g. 111272_112186ins? | GRCh38.p12 | NT_187318.1 | Chr21|NT_1 87318.1 | 67,108 | 68,023 |
| nssv3019455 | Remapped | Pass | NT_187317.1:g.9519 5_96110ins?NT_1873 18.1:g.67108_68023 ins?NT_187388.1:g. 111272_112186ins? | GRCh38.p12 | NT_187317.1 | Chr21|NT_1 87317.1 | 95,195 | 96,110 |
| nssv3019455 | Remapped | Pass | NT_187317.1:g.9519 5_96110ins?NT_1873 18.1:g.67108_68023 ins?NT_187388.1:g. 111272_112186ins? | GRCh38.p12 | NT_187388.1 | Chr22|NT_1 87388.1 | 111,272 | 112,186 |