nsv5613858
- 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: 456 SVs from 23 studies. See in: genome view
Overlapping variant regions from other studies: 454 SVs from 23 studies. See in: genome view
Overlapping variant regions from other studies: 30 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv5613858 | Submitted genomic | GRCh38 (hg38) | Primary Assembly | NC_000023.11 | ChrX | 147,912,049 | 147,912,049 | ||
| nsv5613858 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | Second Pass | NC_000023.10 | ChrX | 146,993,567 | 146,993,567 |
| nsv5613858 | Remapped | Perfect | GRCh37.p13 | PATCHES | First Pass | NW_004070890.2 | ChrX|NW_00 4070890.2 | 3,436,440 | 3,436,440 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv17166471 | Submitted genomic | NC_000023.11:g.147 912049_147912050in s70 | GRCh38 (hg38) | NC_000023.11 | ChrX | 147,912,049 | 147,912,049 | ||
| nssv17166471 | Remapped | Perfect | NW_004070890.2:g.3 436440_3436441ins7 0 | GRCh37.p13 | First Pass | NW_004070890.2 | ChrX|NW_00 4070890.2 | 3,436,440 | 3,436,440 |
| nssv17166471 | Remapped | Perfect | NC_000023.10:g.146 993567_146993568in s70 | GRCh37.p13 | Second Pass | NC_000023.10 | ChrX | 146,993,567 | 146,993,567 |