nsv5520549
- Organism: Homo sapiens
- Study:nstd206 (Byrska-Bishop et al. 2022)
- Variant Type:copy number variation
- Method Type:Sequencing
- Submitted on:GRCh38
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:1,365
- Publication(s):Byrska-Bishop et al. 2022
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: 104 SVs from 28 studies. See in: genome view
Overlapping variant regions from other studies: 104 SVs from 28 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nsv5520549 | Submitted genomic | GRCh38 (hg38) | Primary Assembly | NC_000016.10 | Chr16 | 27,434,661 (-135, +185) | 27,436,025 (-254, +104) | ||
| nsv5520549 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000016.9 | Chr16 | 27,445,982 (-135, +185) | 27,447,346 (-254, +104) |
Variant Call Information
| Variant Call ID | Type | Method | Analysis |
|---|---|---|---|
| nssv17706275 | deletion | Sequencing | Sequence alignment |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv17706275 | Submitted genomic | NC_000016.10:g.(27 434526_27434846)_( 27435771_27436129) del | GRCh38 (hg38) | NC_000016.10 | Chr16 | 27,434,661 (-135, +185) | 27,436,025 (-254, +104) | ||
| nssv17706275 | Remapped | Perfect | NC_000016.9:g.(274 45847_27446167)_(2 7447092_27447450)d el | GRCh37.p13 | First Pass | NC_000016.9 | Chr16 | 27,445,982 (-135, +185) | 27,447,346 (-254, +104) |
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) | Allele Count (AC) | Allele Number (AN) |
|---|---|---|---|
| nssv17706275 | 0.002 | 10 | 6404 |