nsv5289800
- 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:1,925
- 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: 123 SVs from 34 studies. See in: genome view
Overlapping variant regions from other studies: 123 SVs from 34 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nsv5289800 | Submitted genomic | GRCh38.p13 | Primary Assembly | NC_000001.11 | Chr1 | 32,088,771 (-28, +372) | 32,090,695 (-396, +29) | ||
| nsv5289800 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000001.10 | Chr1 | 32,554,372 (-28, +372) | 32,556,296 (-396, +29) |
Variant Call Information
| Variant Call ID | Type | Method | Analysis |
|---|---|---|---|
| nssv16744584 | 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 |
|---|---|---|---|---|---|---|---|---|---|
| nssv16744584 | Submitted genomic | NC_000001.11:g.(32 088743_32089143)_( 32090299_32090724) del | GRCh38.p13 | NC_000001.11 | Chr1 | 32,088,771 (-28, +372) | 32,090,695 (-396, +29) | ||
| nssv16744584 | Remapped | Perfect | NC_000001.10:g.(32 554344_32554744)_( 32555900_32556325) del | GRCh37.p13 | First Pass | NC_000001.10 | Chr1 | 32,554,372 (-28, +372) | 32,556,296 (-396, +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) |
|---|---|
| nssv16744584 | <0.001 |