nsv5671578
- 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: 126 SVs from 20 studies. See in: genome view
Overlapping variant regions from other studies: 124 SVs from 18 studies. See in: genome view
Overlapping variant regions from other studies: 2 SVs from 2 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nsv5671578 | Submitted genomic | GRCh38 (hg38) | Primary Assembly | NC_000020.11 | Chr20 | 36,360,686 | 36,360,686 | ||
| nsv5671578 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | Second Pass | NC_000020.10 | Chr20 | 34,989,089 | 34,989,089 |
| nsv5671578 | Remapped | Perfect | GRCh37.p13 | PATCHES | First Pass | NW_003871095.1 | Chr20|NW_0 03871095.1 | 65,348 | 65,348 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv17116879 | Submitted genomic | NC_000020.11:g.363 60686_36360687ins3 81 | GRCh38 (hg38) | NC_000020.11 | Chr20 | 36,360,686 | 36,360,686 | ||
| nssv17116879 | Remapped | Perfect | NW_003871095.1:g.6 5348_65349ins381 | GRCh37.p13 | First Pass | NW_003871095.1 | Chr20|NW_0 03871095.1 | 65,348 | 65,348 |
| nssv17116879 | Remapped | Perfect | NC_000020.10:g.349 89089_34989090ins3 81 | GRCh37.p13 | Second Pass | NC_000020.10 | Chr20 | 34,989,089 | 34,989,089 |