nsv5641157
- Organism: Homo sapiens
- Study:nstd207 (Ebert et al. 2021)
- Variant Type:insertion
- Method Type:Sequencing
- Submitted on:GRCh38
- Variant Calls:2
- 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: 125 SVs from 23 studies. See in: genome view
Overlapping variant regions from other studies: 125 SVs from 23 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nsv5641157 | Submitted genomic | GRCh38 (hg38) | Primary Assembly | NC_000005.10 | Chr5 | 127,246,857 | 127,246,857 | ||
| nsv5641157 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000005.9 | Chr5 | 126,582,549 | 126,582,549 |
Variant Call Information
| Variant Call ID | Type | Sample ID | Method | Analysis | Other Calls in this Sample and Study |
|---|---|---|---|---|---|
| nssv17126794 | insertion | SAMN00007882 | Sequencing | Sequence alignment | 1,354 |
| nssv17138978 | insertion | HG03065 | Sequencing | Sequence alignment | 3,836 |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv17126794 | Submitted genomic | NC_000005.10:g.127 246857_127246858in s171 | GRCh38 (hg38) | NC_000005.10 | Chr5 | 127,246,857 | 127,246,857 | ||
| nssv17138978 | Submitted genomic | NC_000005.10:g.127 246857_127246858in s545 | GRCh38 (hg38) | NC_000005.10 | Chr5 | 127,246,857 | 127,246,857 | ||
| nssv17126794 | Remapped | Perfect | NC_000005.9:g.1265 82549_126582550ins 171 | GRCh37.p13 | First Pass | NC_000005.9 | Chr5 | 126,582,549 | 126,582,549 |
| nssv17138978 | Remapped | Perfect | NC_000005.9:g.1265 82549_126582550ins 545 | GRCh37.p13 | First Pass | NC_000005.9 | Chr5 | 126,582,549 | 126,582,549 |