nsv4715805
- Organism: Homo sapiens
- Study:nstd195 (Mwapagha et al. 2021)
- Variant Type:translocation
- Method Type:Sequencing
- Submitted on:GRCh37 (hg19)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:1
- Publication(s):Mwapagha 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: 170 SVs from 31 studies. See in: genome view
Overlapping variant regions from other studies: 111 SVs from 22 studies. See in: genome view
Overlapping variant regions from other studies: 170 SVs from 31 studies. See in: genome view
Overlapping variant regions from other studies: 111 SVs from 22 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop | strand |
|---|---|---|---|---|---|---|---|---|---|---|
| nsv4715805 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000010.11 | Chr10 | 54,396,345 | 54,396,345 | - |
| nsv4715805 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000017.11 | Chr17 | 27,127,668 | 27,127,668 | - |
| nsv4715805 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000010.10 | Chr10 | 56,156,105 | 56,156,105 | - | ||
| nsv4715805 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000017.10 | Chr17 | 25,454,694 | 25,454,694 | - |
Variant Call Information
| Variant Call ID | Type | Sample ID | Method | Analysis | Copy number | Other Calls in this Sample and Study |
|---|---|---|---|---|---|---|
| nssv16249731 | interchromosomal translocation | B381 | Sequencing | Paired-end mapping | 1 | 5,743 |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop | strand |
|---|---|---|---|---|---|---|---|---|---|
| nssv16249731 | Remapped | Perfect | GRCh38.p12 | First Pass | NC_000010.11 | Chr10 | 54,396,345 | 54,396,345 | - |
| nssv16249731 | Remapped | Perfect | GRCh38.p12 | First Pass | NC_000017.11 | Chr17 | 27,127,668 | 27,127,668 | - |
| nssv16249731 | Submitted genomic | GRCh37 (hg19) | NC_000010.10 | Chr10 | 56,156,105 | 56,156,105 | - | ||
| nssv16249731 | Submitted genomic | GRCh37 (hg19) | NC_000017.10 | Chr17 | 25,454,694 | 25,454,694 | - |