nsv5612561
- 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: 412 SVs from 29 studies. See in: genome view
Overlapping variant regions from other studies: 409 SVs from 28 studies. See in: genome view
Overlapping variant regions from other studies: 16 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv5612561 | Submitted genomic | GRCh38 (hg38) | Primary Assembly | NC_000023.11 | ChrX | 53,235,874 | 53,235,874 | ||
| nsv5612561 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | Second Pass | NC_000023.10 | ChrX | 53,265,056 | 53,265,056 |
| nsv5612561 | Remapped | Perfect | GRCh37.p13 | PATCHES | First Pass | NW_004070877.1 | ChrX|NW_00 4070877.1 | 2,948,989 | 2,948,989 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv17167659 | Submitted genomic | NC_000023.11:g.532 35874_53235875ins1 499 | GRCh38 (hg38) | NC_000023.11 | ChrX | 53,235,874 | 53,235,874 | ||
| nssv17167659 | Remapped | Perfect | NW_004070877.1:g.2 948989_2948990ins1 499 | GRCh37.p13 | First Pass | NW_004070877.1 | ChrX|NW_00 4070877.1 | 2,948,989 | 2,948,989 |
| nssv17167659 | Remapped | Perfect | NC_000023.10:g.532 65056_53265057ins1 499 | GRCh37.p13 | Second Pass | NC_000023.10 | ChrX | 53,265,056 | 53,265,056 |