nsv5631459
- Organism: Homo sapiens
- Study:nstd207 (Ebert et al. 2021)
- Variant Type:insertion
- Method Type:Sequencing
- Submitted on:GRCh38
- Variant Calls:2
- 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: 111 SVs from 24 studies. See in: genome view
Overlapping variant regions from other studies: 111 SVs from 24 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nsv5631459 | Submitted genomic | GRCh38 (hg38) | Primary Assembly | NC_000005.10 | Chr5 | 81,993,359 | 81,993,359 | ||
| nsv5631459 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000005.9 | Chr5 | 81,289,178 | 81,289,178 |
Variant Call Information
| Variant Call ID | Type | Sample ID | Method | Analysis | Other Calls in this Sample and Study |
|---|---|---|---|---|---|
| nssv17150489 | insertion | SAMN00001695 | Sequencing | Sequence alignment | 6,153 |
| nssv17157675 | insertion | HG03683 | Sequencing | Sequence alignment | 2,232 |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv17150489 | Submitted genomic | NC_000005.10:g.819 93359_81993360ins5 6 | GRCh38 (hg38) | NC_000005.10 | Chr5 | 81,993,359 | 81,993,359 | ||
| nssv17157675 | Submitted genomic | NC_000005.10:g.819 93359_81993360ins2 49 | GRCh38 (hg38) | NC_000005.10 | Chr5 | 81,993,359 | 81,993,359 | ||
| nssv17150489 | Remapped | Perfect | NC_000005.9:g.8128 9178_81289179ins56 | GRCh37.p13 | First Pass | NC_000005.9 | Chr5 | 81,289,178 | 81,289,178 |
| nssv17157675 | Remapped | Perfect | NC_000005.9:g.8128 9178_81289179ins24 9 | GRCh37.p13 | First Pass | NC_000005.9 | Chr5 | 81,289,178 | 81,289,178 |