nsv5313097
- 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:2,811
- 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: 178 SVs from 45 studies. See in: genome view
Overlapping variant regions from other studies: 178 SVs from 45 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nsv5313097 | Submitted genomic | GRCh38.p13 | Primary Assembly | NC_000004.12 | Chr4 | 73,129,801 (-25, +24) | 73,132,611 (-26, +22) | ||
| nsv5313097 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000004.11 | Chr4 | 73,995,518 (-25, +24) | 73,998,328 (-26, +22) |
Variant Call Information
| Variant Call ID | Type | Method | Analysis |
|---|---|---|---|
| nssv16757898 | 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 |
|---|---|---|---|---|---|---|---|---|---|
| nssv16757898 | Submitted genomic | NC_000004.12:g.(73 129776_73129825)_( 73132585_73132633) del | GRCh38.p13 | NC_000004.12 | Chr4 | 73,129,801 (-25, +24) | 73,132,611 (-26, +22) | ||
| nssv16757898 | Remapped | Perfect | NC_000004.11:g.(73 995493_73995542)_( 73998302_73998350) del | GRCh37.p13 | First Pass | NC_000004.11 | Chr4 | 73,995,518 (-25, +24) | 73,998,328 (-26, +22) |
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) |
|---|---|
| nssv16757898 | <0.001 |