nsv5643479
- 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: 127 SVs from 30 studies. See in: genome view
Overlapping variant regions from other studies: 133 SVs from 32 studies. See in: genome view
Overlapping variant regions from other studies: 19 SVs from 10 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nsv5643479 | Submitted genomic | GRCh38 (hg38) | Primary Assembly | NC_000009.12 | Chr9 | 68,326,648 | 68,326,648 | ||
| nsv5643479 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | Second Pass | NC_000009.11 | Chr9 | 70,941,564 | 70,941,564 |
| nsv5643479 | Remapped | Perfect | GRCh37.p13 | PATCHES | First Pass | NW_003871067.1 | Chr9|NW_00 3871067.1 | 106,096 | 106,096 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv17162621 | Submitted genomic | NC_000009.12:g.683 26648_68326649ins3 21 | GRCh38 (hg38) | NC_000009.12 | Chr9 | 68,326,648 | 68,326,648 | ||
| nssv17162621 | Remapped | Perfect | NW_003871067.1:g.1 06096_106097ins321 | GRCh37.p13 | First Pass | NW_003871067.1 | Chr9|NW_00 3871067.1 | 106,096 | 106,096 |
| nssv17162621 | Remapped | Perfect | NC_000009.11:g.709 41564_70941565ins3 21 | GRCh37.p13 | Second Pass | NC_000009.11 | Chr9 | 70,941,564 | 70,941,564 |