nsv6290024
- Organism: Homo sapiens
- Study:nstd217 (Zhang et al. 2022)
- Variant Type:sequence alteration
- Method Type:Sequencing
- Submitted on:GRCh38
- Variant is Defined by:LC474859.1
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:3,072
- Publication(s):Zhang et al. 2022
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: 728 SVs from 72 studies. See in: genome view
Overlapping variant regions from other studies: 728 SVs from 72 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nsv6290024 | Submitted genomic | GRCh38 (hg38) | Primary Assembly | NC_000006.12 | Chr6 | 29,942,447 | 29,945,518 | ||
| nsv6290024 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000006.11 | Chr6 | 29,910,224 | 29,913,295 |
Variant Call Information
| Variant Call ID | Type | Sample ID | Method | Analysis |
|---|---|---|---|---|
| nssv17955694 | sequence alteration | 17ZZ2298 | Sequencing | Sequence alignment |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|
| nssv17955694 | Submitted genomic | GRCh38 (hg38) | NC_000006.12 | Chr6 | 29,942,447 | 29,945,518 | ||
| nssv17955694 | Remapped | Perfect | GRCh37.p13 | First Pass | NC_000006.11 | Chr6 | 29,910,224 | 29,913,295 |