nsv3169077
- Organism: Homo sapiens
- Study:nstd158 (Cleal et al. 2019)
- Variant Type:translocation
- Method Type:Sequencing
- Submitted on:GRCh37 (hg19)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:1
- Publication(s):Cleal et al. 2019
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: 107 SVs from 23 studies. See in: genome view
Overlapping variant regions from other studies: 1 SVs from 1 studies. See in: genome view
Overlapping variant regions from other studies: 107 SVs from 23 studies. See in: genome view
Overlapping variant regions from other studies: 11 SVs from 4 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 |
|---|---|---|---|---|---|---|---|---|---|---|
| nsv3169077 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000005.10 | Chr5 | 132,909,916 (-569, +569) | 132,909,916 (-569, +569) | + |
| nsv3169077 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NT_167214.1 | Unplaced|N T_167214.1 | 143,767 (-569, +569) | 143,767 (-569, +569) | + |
| nsv3169077 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000005.9 | Chr5 | 132,245,608 (-569, +569) | 132,245,608 (-569, +569) | + | ||
| nsv3169077 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NT_167214.1 | Unplaced|N T_167214.1 | 143,767 (-569, +569) | 143,767 (-569, +569) | + |
Variant Call Information
| Variant Call ID | Type | Sample ID | Method | Analysis | Other Calls in this Sample and Study |
|---|---|---|---|---|---|
| nssv14240363 | interchromosomal translocation | DB96 | Sequencing | Paired-end mapping | 19 |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop | strand |
|---|---|---|---|---|---|---|---|---|---|
| nssv14240363 | Remapped | Perfect | GRCh38.p12 | First Pass | NC_000005.10 | Chr5 | 132,909,916 (-569, +569) | 132,909,916 (-569, +569) | + |
| nssv14240363 | Remapped | Perfect | GRCh38.p12 | First Pass | NT_167214.1 | Unplaced|N T_167214.1 | 143,767 (-569, +569) | 143,767 (-569, +569) | + |
| nssv14240363 | Submitted genomic | GRCh37 (hg19) | NC_000005.9 | Chr5 | 132,245,608 (-569, +569) | 132,245,608 (-569, +569) | + | ||
| nssv14240363 | Submitted genomic | GRCh37 (hg19) | NT_167214.1 | Unplaced|N T_167214.1 | 143,767 (-569, +569) | 143,767 (-569, +569) | + |