nsv5621388
- 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: 439 SVs from 19 studies. See in: genome view
Overlapping variant regions from other studies: 437 SVs from 19 studies. See in: genome view
Overlapping variant regions from other studies: 27 SVs from 7 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nsv5621388 | Submitted genomic | GRCh38 (hg38) | Primary Assembly | NC_000023.11 | ChrX | 148,808,828 | 148,808,828 | ||
| nsv5621388 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | Second Pass | NC_000023.10 | ChrX | 147,890,352 | 147,890,352 |
| nsv5621388 | Remapped | Perfect | GRCh37.p13 | PATCHES | First Pass | NW_004070890.2 | ChrX|NW_00 4070890.2 | 4,333,225 | 4,333,225 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv17166494 | Submitted genomic | NC_000023.11:g.148 808828_148808829in s7625 | GRCh38 (hg38) | NC_000023.11 | ChrX | 148,808,828 | 148,808,828 | ||
| nssv17166494 | Remapped | Perfect | NW_004070890.2:g.4 333225_4333226ins7 625 | GRCh37.p13 | First Pass | NW_004070890.2 | ChrX|NW_00 4070890.2 | 4,333,225 | 4,333,225 |
| nssv17166494 | Remapped | Perfect | NC_000023.10:g.147 890352_147890353in s7625 | GRCh37.p13 | Second Pass | NC_000023.10 | ChrX | 147,890,352 | 147,890,352 |