nsv4763531
- Organism: Homo sapiens
- Study:nstd199 (Quan et al. 2021)
- Variant Type:inversion
- Method Type:Sequencing
- Submitted on:GRCh37
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:35,074,507
- Publication(s):Quan 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: 97759 SVs from 149 studies. See in: genome view
Overlapping variant regions from other studies: 97499 SVs from 149 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nsv4763531 | Remapped | Good | GRCh38.p12 | Primary Assembly | First Pass | NC_000007.14 | Chr7 | 67,304,386 | 102,378,892 |
| nsv4763531 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000007.13 | Chr7 | 66,769,373 | 102,019,339 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis |
|---|---|---|---|
| nssv16287256 | inversion | Sequencing | Split read mapping |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv16287256 | Remapped | Good | NC_000007.14:g.673 04386_102378892inv | GRCh38.p12 | First Pass | NC_000007.14 | Chr7 | 67,304,386 | 102,378,892 |
| nssv16287256 | Submitted genomic | NC_000007.13:g.667 69373_102019339inv | GRCh37 (hg19) | NC_000007.13 | Chr7 | 66,769,373 | 102,019,339 |