nsv5906200
- 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:537,408
- 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: 2761 SVs from 110 studies. See in: genome view
Overlapping variant regions from other studies: 2766 SVs from 110 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nsv5906200 | Submitted genomic | GRCh38 (hg38) | Primary Assembly | NC_000004.12 | Chr4 | 9,159,413 | 9,696,820 | ||
| nsv5906200 | Remapped | Good | GRCh37.p13 | Primary Assembly | First Pass | NC_000004.11 | Chr4 | 9,161,139 | 9,698,444 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis |
|---|---|---|---|
| nssv17419660 | deletion | Sequencing | Sequence alignment |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv17419660 | Submitted genomic | NC_000004.12:g.915 9413_9696820del | GRCh38 (hg38) | NC_000004.12 | Chr4 | 9,159,413 | 9,696,820 | ||
| nssv17419660 | Remapped | Good | NC_000004.11:g.916 1139_9698444del | GRCh37.p13 | First Pass | NC_000004.11 | Chr4 | 9,161,139 | 9,698,444 |