nsv5547669
- 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:1,214
- 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: 118 SVs from 32 studies. See in: genome view
Overlapping variant regions from other studies: 118 SVs from 32 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nsv5547669 | Submitted genomic | GRCh38 (hg38) | Primary Assembly | NC_000022.11 | Chr22 | 31,641,613 (-65, +40) | 31,642,826 (-20, +66) | ||
| nsv5547669 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000022.10 | Chr22 | 32,037,599 (-65, +40) | 32,038,812 (-20, +66) |
Variant Call Information
| Variant Call ID | Type | Method | Analysis |
|---|---|---|---|
| nssv17728505 | deletion | Sequencing | Sequence alignment |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv17728505 | Submitted genomic | NC_000022.11:g.(31 641548_31641653)_( 31642806_31642892) del | GRCh38 (hg38) | NC_000022.11 | Chr22 | 31,641,613 (-65, +40) | 31,642,826 (-20, +66) | ||
| nssv17728505 | Remapped | Perfect | NC_000022.10:g.(32 037534_32037639)_( 32038792_32038878) del | GRCh37.p13 | First Pass | NC_000022.10 | Chr22 | 32,037,599 (-65, +40) | 32,038,812 (-20, +66) |
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) |
|---|---|---|---|
| nssv17728505 | 0.036 | 228 | 6404 |