nsv5641723
- 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: 249 SVs from 29 studies. See in: genome view
Overlapping variant regions from other studies: 233 SVs from 27 studies. See in: genome view
Overlapping variant regions from other studies: 37 SVs from 11 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nsv5641723 | Submitted genomic | GRCh38 (hg38) | Primary Assembly | NC_000008.11 | Chr8 | 143,808,288 | 143,808,288 | ||
| nsv5641723 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | Second Pass | NC_000008.10 | Chr8 | 144,890,458 | 144,890,458 |
| nsv5641723 | Remapped | Perfect | GRCh37.p13 | PATCHES | First Pass | NW_003315923.1 | Chr8|NW_00 3315923.1 | 146,933 | 146,933 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv17155324 | Submitted genomic | NC_000008.11:g.143 808288_143808289in s83 | GRCh38 (hg38) | NC_000008.11 | Chr8 | 143,808,288 | 143,808,288 | ||
| nssv17155324 | Remapped | Perfect | NW_003315923.1:g.1 46933_146934ins83 | GRCh37.p13 | First Pass | NW_003315923.1 | Chr8|NW_00 3315923.1 | 146,933 | 146,933 |
| nssv17155324 | Remapped | Perfect | NC_000008.10:g.144 890458_144890459in s83 | GRCh37.p13 | Second Pass | NC_000008.10 | Chr8 | 144,890,458 | 144,890,458 |