nsv5889315
- Organism: Homo sapiens
- Study:nstd209 (Almarri et al. 2020)
- Variant Type:copy number variation
- Method Type:Sequencing
- Submitted on:GRCh38
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:311
- Publication(s):Almarri et al. 2020
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: 259 SVs from 30 studies. See in: genome view
Overlapping variant regions from other studies: 259 SVs from 30 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nsv5889315 | Submitted genomic | GRCh38 (hg38) | Primary Assembly | NC_000005.10 | Chr5 | 16,698,611 | 16,698,921 | ||
| nsv5889315 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000005.9 | Chr5 | 16,698,720 | 16,699,030 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis |
|---|---|---|---|
| nssv17421759 | deletion | Sequencing | Sequence alignment |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv17421759 | Submitted genomic | NC_000005.10:g.166 98611_16698921del | GRCh38 (hg38) | NC_000005.10 | Chr5 | 16,698,611 | 16,698,921 | ||
| nssv17421759 | Remapped | Perfect | NC_000005.9:g.1669 8720_16699030del | GRCh37.p13 | First Pass | NC_000005.9 | Chr5 | 16,698,720 | 16,699,030 |