nsv5205738
- 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:337
- 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: 272 SVs from 43 studies. See in: genome view
Overlapping variant regions from other studies: 272 SVs from 43 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nsv5205738 | Submitted genomic | GRCh38.p13 | Primary Assembly | NC_000018.10 | Chr18 | 46,802,760 | 46,803,096 | ||
| nsv5205738 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000018.9 | Chr18 | 44,382,723 | 44,383,059 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis |
|---|---|---|---|
| nssv16759236 | 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 |
|---|---|---|---|---|---|---|---|---|---|
| nssv16759236 | Submitted genomic | NC_000018.10:g.468 02760_46803096del | GRCh38.p13 | NC_000018.10 | Chr18 | 46,802,760 | 46,803,096 | ||
| nssv16759236 | Remapped | Perfect | NC_000018.9:g.4438 2723_44383059del | GRCh37.p13 | First Pass | NC_000018.9 | Chr18 | 44,382,723 | 44,383,059 |
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) |
|---|---|
| nssv16759236 | 0.071 |