nsv479412
- Organism: Homo sapiens
- Study:nstd35 (Kidd et al. 2010)
- Variant Type:novel sequence insertion
- Method Type:Sequencing
- Variant is Defined by:GU266917
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:2,260
- 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
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|
| nsv479412 | Remapped | Good | GRCh38.p12 | Primary Assembly | NT_011362.11 | Chr20|NT_0 11362.11 | 24,492,322 | 24,494,581 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis |
|---|---|---|---|
| nssv3017933 | 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 |
|---|---|---|---|---|---|---|---|---|
| nssv3017933 | Remapped | Good | NT_011362.11:g.244 92322_24494581ins? | GRCh38.p12 | NT_011362.11 | Chr20|NT_0 11362.11 | 24,492,322 | 24,494,581 |