nsv5326903
- 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:10,892
- 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: 102 SVs from 23 studies. See in: genome view
Overlapping variant regions from other studies: 102 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv5326903 | Submitted genomic | GRCh38.p13 | Primary Assembly | NC_000022.11 | Chr22 | 38,792,425 (-30, +262) | 38,803,316 (-194, +29) | ||
| nsv5326903 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000022.10 | Chr22 | 39,188,430 (-30, +262) | 39,199,321 (-194, +29) |
Variant Call Information
| Variant Call ID | Type | Method | Analysis |
|---|---|---|---|
| nssv16758730 | 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 |
|---|---|---|---|---|---|---|---|---|---|
| nssv16758730 | Submitted genomic | NC_000022.11:g.(38 792395_38792687)_( 38803122_38803345) del | GRCh38.p13 | NC_000022.11 | Chr22 | 38,792,425 (-30, +262) | 38,803,316 (-194, +29) | ||
| nssv16758730 | Remapped | Perfect | NC_000022.10:g.(39 188400_39188692)_( 39199127_39199350) del | GRCh37.p13 | First Pass | NC_000022.10 | Chr22 | 39,188,430 (-30, +262) | 39,199,321 (-194, +29) |
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) |
|---|---|
| nssv16758730 | <0.001 |