nsv5627242
- Organism: Homo sapiens
- Study:nstd207 (Ebert et al. 2021)
- Variant Type:insertion
- Method Type:Sequencing
- Submitted on:GRCh38
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:1
- Publication(s):Ebert et al. 2021
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: 218 SVs from 31 studies. See in: genome view
Overlapping variant regions from other studies: 207 SVs from 30 studies. See in: genome view
Overlapping variant regions from other studies: 11 SVs from 8 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nsv5627242 | Submitted genomic | GRCh38 (hg38) | Primary Assembly | NC_000008.11 | Chr8 | 142,639,398 | 142,639,398 | ||
| nsv5627242 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | Second Pass | NC_000008.10 | Chr8 | 143,720,751 | 143,720,751 |
| nsv5627242 | Remapped | Perfect | GRCh37.p13 | PATCHES | First Pass | NW_003871066.2 | Chr8|NW_00 3871066.2 | 9,531 | 9,531 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv17149474 | Submitted genomic | NC_000008.11:g.142 639398_142639399in s121 | GRCh38 (hg38) | NC_000008.11 | Chr8 | 142,639,398 | 142,639,398 | ||
| nssv17149474 | Remapped | Perfect | NW_003871066.2:g.9 531_9532ins121 | GRCh37.p13 | First Pass | NW_003871066.2 | Chr8|NW_00 3871066.2 | 9,531 | 9,531 |
| nssv17149474 | Remapped | Perfect | NC_000008.10:g.143 720751_143720752in s121 | GRCh37.p13 | Second Pass | NC_000008.10 | Chr8 | 143,720,751 | 143,720,751 |