nsv5207655
- 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:1,531,700
- 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: 3840 SVs from 111 studies. See in: genome view
Overlapping variant regions from other studies: 3841 SVs from 111 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nsv5207655 | Submitted genomic | GRCh38.p13 | Primary Assembly | NC_000002.12 | Chr2 | 182,398,101 | 183,929,800 | ||
| nsv5207655 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000002.11 | Chr2 | 183,262,828 | 184,794,527 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis |
|---|---|---|---|
| nssv16851173 | copy number variation | Sequencing | Read depth |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|
| nssv16851173 | Submitted genomic | GRCh38.p13 | NC_000002.12 | Chr2 | 182,398,101 | 183,929,800 | ||
| nssv16851173 | Remapped | Perfect | GRCh37.p13 | First Pass | NC_000002.11 | Chr2 | 183,262,828 | 184,794,527 |