nsv5553433
- Organism: Homo sapiens
- Study:nstd206 (Byrska-Bishop et al. 2022)
- Variant Type:insertion
- Method Type:Sequencing
- Submitted on:GRCh38
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:16
- 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: 135 SVs from 29 studies. See in: genome view
Overlapping variant regions from other studies: 137 SVs from 30 studies. See in: genome view
Overlapping variant regions from other studies: 10 SVs from 8 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nsv5553433 | Submitted genomic | GRCh38 (hg38) | Primary Assembly | NC_000001.11 | Chr1 | 206,069,713 | 206,069,728 | ||
| nsv5553433 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | Second Pass | NC_000001.10 | Chr1 | 206,271,604 | 206,271,619 |
| nsv5553433 | Remapped | Perfect | GRCh37.p13 | PATCHES | First Pass | NW_003871057.1 | Chr1|NW_00 3871057.1 | 60,567 | 60,582 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis |
|---|---|---|---|
| nssv16895280 | insertion | Sequencing | Sequence alignment |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv16895280 | Submitted genomic | NC_000001.11:g.206 069713_206069728in s316 | GRCh38 (hg38) | NC_000001.11 | Chr1 | 206,069,713 | 206,069,728 | ||
| nssv16895280 | Remapped | Perfect | NW_003871057.1:g.6 0567_60582ins316 | GRCh37.p13 | First Pass | NW_003871057.1 | Chr1|NW_00 3871057.1 | 60,567 | 60,582 |
| nssv16895280 | Remapped | Perfect | NC_000001.10:g.206 271604_206271619in s316 | GRCh37.p13 | Second Pass | NC_000001.10 | Chr1 | 206,271,604 | 206,271,619 |
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) |
|---|---|---|---|
| nssv16895280 | 0.001 | 8 | 6404 |