nsv5532277
- 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:2,610
- 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: 225 SVs from 23 studies. See in: genome view
Overlapping variant regions from other studies: 225 SVs from 23 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nsv5532277 | Submitted genomic | GRCh38 (hg38) | Primary Assembly | NC_000018.10 | Chr18 | 12,693,647 (-111, +282) | 12,696,256 (-285, +74) | ||
| nsv5532277 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000018.9 | Chr18 | 12,693,646 (-111, +282) | 12,696,255 (-285, +74) |
Variant Call Information
| Variant Call ID | Type | Method | Analysis |
|---|---|---|---|
| nssv17716325 | deletion | Sequencing | Sequence alignment |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv17716325 | Submitted genomic | NC_000018.10:g.(12 693536_12693929)_( 12695971_12696330) del | GRCh38 (hg38) | NC_000018.10 | Chr18 | 12,693,647 (-111, +282) | 12,696,256 (-285, +74) | ||
| nssv17716325 | Remapped | Perfect | NC_000018.9:g.(126 93535_12693928)_(1 2695970_12696329)d el | GRCh37.p13 | First Pass | NC_000018.9 | Chr18 | 12,693,646 (-111, +282) | 12,696,255 (-285, +74) |
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) |
|---|---|---|---|
| nssv17716325 | <0.001 | 1 | 6404 |