nsv5658107
- 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: 86 SVs from 25 studies. See in: genome view
Overlapping variant regions from other studies: 80 SVs from 23 studies. See in: genome view
Overlapping variant regions from other studies: 9 SVs from 9 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nsv5658107 | Submitted genomic | GRCh38 (hg38) | Primary Assembly | NC_000011.10 | Chr11 | 69,813,600 | 69,813,600 | ||
| nsv5658107 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | Second Pass | NC_000011.9 | Chr11 | 69,628,368 | 69,628,368 |
| nsv5658107 | Remapped | Perfect | GRCh37.p13 | PATCHES | First Pass | NW_003571046.1 | Chr11|NW_0 03571046.1 | 13,583 | 13,583 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv17075803 | Submitted genomic | NC_000011.10:g.698 13600_69813601ins7 3 | GRCh38 (hg38) | NC_000011.10 | Chr11 | 69,813,600 | 69,813,600 | ||
| nssv17075803 | Remapped | Perfect | NW_003571046.1:g.1 3583_13584ins73 | GRCh37.p13 | First Pass | NW_003571046.1 | Chr11|NW_0 03571046.1 | 13,583 | 13,583 |
| nssv17075803 | Remapped | Perfect | NC_000011.9:g.6962 8368_69628369ins73 | GRCh37.p13 | Second Pass | NC_000011.9 | Chr11 | 69,628,368 | 69,628,368 |