nsv513679
- Organism: Homo sapiens
- Study:nstd50 (Arlt et al. 2011)
- Variant Type:inversion
- Method Type:Sequencing
- Submitted on:NCBI36 (hg18)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:5,120
- Publication(s):Arlt et al. 2011
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: 157 SVs from 41 studies. See in: genome view
Overlapping variant regions from other studies: 157 SVs from 41 studies. See in: genome view
Overlapping variant regions from other studies: 53 SVs from 17 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Outer Start | Outer Stop |
|---|---|---|---|---|---|---|---|---|---|
| nsv513679 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000007.14 | Chr7 | 107,417,248 | 107,422,367 |
| nsv513679 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000007.13 | Chr7 | 107,057,693 | 107,062,812 |
| nsv513679 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000007.12 | Chr7 | 106,844,929 | 106,850,048 |
Variant Call Information
| Variant Call ID | Type | Sample ID | Method | Analysis | Other Calls in this Sample and Study |
|---|---|---|---|---|---|
| nssv626931 | inversion | 1 | Sequencing | Paired-end mapping | 2,637 |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Outer Start | Outer Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv626931 | Remapped | Perfect | NC_000007.14:g.(10 7417248_?)_(?_1074 22367)inv5120 | GRCh38.p12 | First Pass | NC_000007.14 | Chr7 | 107,417,248 | 107,422,367 |
| nssv626931 | Remapped | Perfect | NC_000007.13:g.(10 7057693_?)_(?_1070 62812)inv5120 | GRCh37.p13 | First Pass | NC_000007.13 | Chr7 | 107,057,693 | 107,062,812 |
| nssv626931 | Submitted genomic | NC_000007.12:g.(10 6844929_?)_(?_1068 50048)inv5120 | NCBI36 (hg18) | NC_000007.12 | Chr7 | 106,844,929 | 106,850,048 |