nsv513685
- 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:7,436
- 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: 285 SVs from 42 studies. See in: genome view
Overlapping variant regions from other studies: 285 SVs from 42 studies. See in: genome view
Overlapping variant regions from other studies: 80 SVs from 13 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv513685 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000008.11 | Chr8 | 117,995,786 | 118,003,221 |
| nsv513685 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000008.10 | Chr8 | 119,008,025 | 119,015,460 |
| nsv513685 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000008.9 | Chr8 | 119,077,206 | 119,084,641 |
Variant Call Information
| Variant Call ID | Type | Sample ID | Method | Analysis | Other Calls in this Sample and Study |
|---|---|---|---|---|---|
| nssv626937 | 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 |
|---|---|---|---|---|---|---|---|---|---|
| nssv626937 | Remapped | Perfect | NC_000008.11:g.(11 7995786_?)_(?_1180 03221)inv7436 | GRCh38.p12 | First Pass | NC_000008.11 | Chr8 | 117,995,786 | 118,003,221 |
| nssv626937 | Remapped | Perfect | NC_000008.10:g.(11 9008025_?)_(?_1190 15460)inv7436 | GRCh37.p13 | First Pass | NC_000008.10 | Chr8 | 119,008,025 | 119,015,460 |
| nssv626937 | Submitted genomic | NC_000008.9:g.(119 077206_?)_(?_11908 4641)inv7436 | NCBI36 (hg18) | NC_000008.9 | Chr8 | 119,077,206 | 119,084,641 |