nsv5327792
- Organism: Homo sapiens
- Study:nstd204 (Chen et al. 2021)
- Variant Type:translocation
- Method Type:Sequencing
- Submitted on:GRCh38
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:1
- Publication(s):Chen 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: 115 SVs from 25 studies. See in: genome view
Overlapping variant regions from other studies: 94 SVs from 20 studies. See in: genome view
Overlapping variant regions from other studies: 115 SVs from 25 studies. See in: genome view
Overlapping variant regions from other studies: 85 SVs from 17 studies. See in: genome view
Overlapping variant regions from other studies: 11 SVs from 8 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 |
|---|---|---|---|---|---|---|---|---|---|---|
| nsv5327792 | Submitted genomic | GRCh38.p13 | Primary Assembly | NC_000006.12 | Chr6 | 93,120,193 | 93,120,193 | + | ||
| nsv5327792 | Submitted genomic | GRCh38.p13 | Primary Assembly | NC_000017.11 | Chr17 | 28,467,782 | 28,467,782 | + | ||
| nsv5327792 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000006.11 | Chr6 | 93,829,911 | 93,829,911 | + |
| nsv5327792 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | Second Pass | NC_000017.10 | Chr17 | 26,794,800 | 26,794,800 | + |
| nsv5327792 | Remapped | Perfect | GRCh37.p13 | PATCHES | First Pass | NW_003871090.1 | Chr17|NW_0 03871090.1 | 149,643 | 149,643 | + |
Variant Call Information
| Variant Call ID | Type | Method | Analysis |
|---|---|---|---|
| nssv16755323 | interchromosomal translocation | Sequencing | Split read and paired-end mapping |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop | strand |
|---|---|---|---|---|---|---|---|---|---|
| nssv16755323 | Submitted genomic | GRCh38.p13 | NC_000006.12 | Chr6 | 93,120,193 | 93,120,193 | + | ||
| nssv16755323 | Submitted genomic | GRCh38.p13 | NC_000017.11 | Chr17 | 28,467,782 | 28,467,782 | + | ||
| nssv16755323 | Remapped | Perfect | GRCh37.p13 | First Pass | NC_000006.11 | Chr6 | 93,829,911 | 93,829,911 | + |
| nssv16755323 | Remapped | Perfect | GRCh37.p13 | First Pass | NW_003871090.1 | Chr17|NW_0 03871090.1 | 149,643 | 149,643 | + |
| nssv16755323 | Remapped | Perfect | GRCh37.p13 | Second Pass | NC_000017.10 | Chr17 | 26,794,800 | 26,794,800 | + |
No validation data were submitted for this variant
No clinical assertion data were submitted for this variant
Complete genotype and/or allele frequency data for this study can be found on dbVar's FTP site.
Genotype Information
| Variant Call ID | Allele Frequency (AF) |
|---|---|
| nssv16755323 | <0.001 |