nsv5216514
- Organism: Homo sapiens
- Study:nstd204 (Chen et al. 2021)
- Variant Type:mobile element deletion
- Method Type:Sequencing
- Submitted on:GRCh38
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:323
- 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: 147 SVs from 26 studies. See in: genome view
Overlapping variant regions from other studies: 147 SVs from 26 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nsv5216514 | Submitted genomic | GRCh38.p13 | Primary Assembly | NC_000012.12 | Chr12 | 9,059,999 (-29, +28) | 9,060,321 (-29, +28) | ||
| nsv5216514 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000012.11 | Chr12 | 9,212,595 (-29, +28) | 9,212,917 (-29, +28) |
Variant Call Information
| Variant Call ID | Type | Method | Analysis |
|---|---|---|---|
| nssv16749187 | alu deletion | Sequencing | Split read and paired-end mapping |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv16749187 | Submitted genomic | NC_000012.12:g.(90 59970_9060027)_(90 60292_9060349)del | GRCh38.p13 | NC_000012.12 | Chr12 | 9,059,999 (-29, +28) | 9,060,321 (-29, +28) | ||
| nssv16749187 | Remapped | Perfect | NC_000012.11:g.(92 12566_9212623)_(92 12888_9212945)del | GRCh37.p13 | First Pass | NC_000012.11 | Chr12 | 9,212,595 (-29, +28) | 9,212,917 (-29, +28) |
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) |
|---|---|
| nssv16749187 | <0.001 |