nsv513670
- 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:24,258
- 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: 414 SVs from 69 studies. See in: genome view
Overlapping variant regions from other studies: 414 SVs from 69 studies. See in: genome view
Overlapping variant regions from other studies: 190 SVs from 21 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv513670 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000006.12 | Chr6 | 167,242,119 | 167,266,376 |
| nsv513670 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000006.11 | Chr6 | 167,655,607 | 167,679,864 |
| nsv513670 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000006.10 | Chr6 | 167,575,597 | 167,599,854 |
Variant Call Information
| Variant Call ID | Type | Sample ID | Method | Analysis | Other Calls in this Sample and Study |
|---|---|---|---|---|---|
| nssv626922 | 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 |
|---|---|---|---|---|---|---|---|---|---|
| nssv626922 | Remapped | Perfect | NC_000006.12:g.(16 7242119_?)_(?_1672 66376)inv24258 | GRCh38.p12 | First Pass | NC_000006.12 | Chr6 | 167,242,119 | 167,266,376 |
| nssv626922 | Remapped | Perfect | NC_000006.11:g.(16 7655607_?)_(?_1676 79864)inv24258 | GRCh37.p13 | First Pass | NC_000006.11 | Chr6 | 167,655,607 | 167,679,864 |
| nssv626922 | Submitted genomic | NC_000006.10:g.(16 7575597_?)_(?_1675 99854)inv24258 | NCBI36 (hg18) | NC_000006.10 | Chr6 | 167,575,597 | 167,599,854 |