nsv3971578
- Organism: Homo sapiens
- Study:nstd168 (Levy-Sakin et al. 2019)
- Variant Type:translocation
- Method Type:Optical mapping
- Submitted on:GRCh38 (hg38)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:1
- Publication(s):Levy-Sakin 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: 409 SVs from 29 studies. See in: genome view
Overlapping variant regions from other studies: 369 SVs from 20 studies. See in: genome view
Overlapping variant regions from other studies: 409 SVs from 29 studies. See in: genome view
Overlapping variant regions from other studies: 370 SVs from 20 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 |
|---|---|---|---|---|---|---|---|---|---|---|
| nsv3971578 | Submitted genomic | GRCh38 (hg38) | Primary Assembly | NC_000023.11 | ChrX | 89,231,749 | 89,231,749 | + | ||
| nsv3971578 | Submitted genomic | GRCh38 (hg38) | Primary Assembly | NC_000024.10 | ChrY | 6,579,406 | 6,579,406 | + | ||
| nsv3971578 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000023.10 | ChrX | 88,486,748 | 88,486,748 | + |
| nsv3971578 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000024.9 | ChrY | 6,447,447 | 6,447,447 | + |
Variant Call Information
| Variant Call ID | Type | Method | Analysis |
|---|---|---|---|
| nssv15210747 | interchromosomal translocation | Optical mapping | Optical mapping |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop | strand |
|---|---|---|---|---|---|---|---|---|---|
| nssv15210747 | Submitted genomic | GRCh38 (hg38) | NC_000023.11 | ChrX | 89,231,749 | 89,231,749 | + | ||
| nssv15210747 | Submitted genomic | GRCh38 (hg38) | NC_000024.10 | ChrY | 6,579,406 | 6,579,406 | + | ||
| nssv15210747 | Remapped | Perfect | GRCh37.p13 | First Pass | NC_000023.10 | ChrX | 88,486,748 | 88,486,748 | + |
| nssv15210747 | Remapped | Perfect | GRCh37.p13 | First Pass | NC_000024.9 | ChrY | 6,447,447 | 6,447,447 | + |