nsv5310120
- Organism: Homo sapiens
- Study:nstd204 (Chen et al. 2021)
- Variant Type:copy number variation
- Method Type:Sequencing
- Submitted on:GRCh38
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:5,437
- 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: 416 SVs from 47 studies. See in: genome view
Overlapping variant regions from other studies: 415 SVs from 47 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nsv5310120 | Submitted genomic | GRCh38.p13 | Primary Assembly | NC_000017.11 | Chr17 | 737,670 (-6, +333) | 743,106 (-331, +9) | ||
| nsv5310120 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000017.10 | Chr17 | 640,910 (-6, +333) | 646,346 (-331, +9) |
Variant Call Information
| Variant Call ID | Type | Method | Analysis |
|---|---|---|---|
| nssv16741686 | 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 |
|---|---|---|---|---|---|---|---|---|---|
| nssv16741686 | Submitted genomic | NC_000017.11:g.(73 7664_738003)_(7427 75_743115)del | GRCh38.p13 | NC_000017.11 | Chr17 | 737,670 (-6, +333) | 743,106 (-331, +9) | ||
| nssv16741686 | Remapped | Perfect | NC_000017.10:g.(64 0904_641243)_(6460 15_646355)del | GRCh37.p13 | First Pass | NC_000017.10 | Chr17 | 640,910 (-6, +333) | 646,346 (-331, +9) |
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) |
|---|---|
| nssv16741686 | <0.001 |