nsv2816770
- Organism: Homo sapiens
- Study:nstd137 (Huddleston et al. 2016)
- Variant Type:inversion
- Method Type:Sequencing
- Submitted on:GRCh38 (hg38)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:887
- Publication(s):Huddleston et al. 2016
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: 135 SVs from 40 studies. See in: genome view
Overlapping variant regions from other studies: 135 SVs from 40 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nsv2816770 | Submitted genomic | GRCh38 (hg38) | Primary Assembly | NC_000007.14 | Chr7 | 67,019,451 | 67,020,337 | ||
| nsv2816770 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000007.13 | Chr7 | 66,484,438 | 66,485,324 |
Variant Call Information
| Variant Call ID | Type | Sample ID | Method | Analysis | Other Calls in this Sample and Study |
|---|---|---|---|---|---|
| nssv13701154 | inversion | SAMN03255769 | Sequencing | Local sequence assembly | 46 |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv13701154 | Submitted genomic | NC_000007.14:g.670 19451_67020337inv | GRCh38 (hg38) | NC_000007.14 | Chr7 | 67,019,451 | 67,020,337 | ||
| nssv13701154 | Remapped | Perfect | NC_000007.13:g.664 84438_66485324inv | GRCh37.p13 | First Pass | NC_000007.13 | Chr7 | 66,484,438 | 66,485,324 |