nsv6315005
- Organism: Homo sapiens
- Study:nstd221 (Bao et al. 2022b)
- Variant Type:copy number variation
- Method Type:Sequencing
- Submitted on:GRCh38
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:81,149
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: 1209 SVs from 85 studies. See in: genome view
Overlapping variant regions from other studies: 1209 SVs from 85 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nsv6315005 | Submitted genomic | GRCh38 (hg38) | Primary Assembly | NC_000016.10 | Chr16 | 157,989 | 239,137 | ||
| nsv6315005 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000016.9 | Chr16 | 207,988 | 289,136 |
Variant Call Information
| Variant Call ID | Type | Sample ID | Method | Analysis |
|---|---|---|---|---|
| nssv17976487 | deletion | FXH | Sequencing | Sequence alignment |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv17976487 | Submitted genomic | NC_000016.10:g.157 989_239137del | GRCh38 (hg38) | NC_000016.10 | Chr16 | 157,989 | 239,137 | ||
| nssv17976487 | Remapped | Perfect | NC_000016.9:g.2079 88_289136del | GRCh37.p13 | First Pass | NC_000016.9 | Chr16 | 207,988 | 289,136 |