nsv5641151
- 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: 118 SVs from 27 studies. See in: genome view
Overlapping variant regions from other studies: 116 SVs from 27 studies. See in: genome view
Overlapping variant regions from other studies: 7 SVs from 6 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nsv5641151 | Submitted genomic | GRCh38 (hg38) | Primary Assembly | NC_000007.14 | Chr7 | 130,591,453 | 130,591,453 | ||
| nsv5641151 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | Second Pass | NC_000007.13 | Chr7 | 130,276,331 | 130,276,331 |
| nsv5641151 | Remapped | Perfect | GRCh37.p13 | PATCHES | First Pass | NW_003871065.1 | Chr7|NW_00 3871065.1 | 270,684 | 270,684 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv17158910 | Submitted genomic | NC_000007.14:g.130 591453_130591454in s195 | GRCh38 (hg38) | NC_000007.14 | Chr7 | 130,591,453 | 130,591,453 | ||
| nssv17158910 | Remapped | Perfect | NW_003871065.1:g.2 70684_270685ins195 | GRCh37.p13 | First Pass | NW_003871065.1 | Chr7|NW_00 3871065.1 | 270,684 | 270,684 |
| nssv17158910 | Remapped | Perfect | NC_000007.13:g.130 276331_130276332in s195 | GRCh37.p13 | Second Pass | NC_000007.13 | Chr7 | 130,276,331 | 130,276,331 |