nsv512883
- Organism: Homo sapiens
- Study:nstd50 (Arlt et al. 2011)
- Variant Type:insertion
- Method Type:Sequencing
- Submitted on:NCBI36 (hg18)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:2,384
- 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: 136 SVs from 29 studies. See in: genome view
Overlapping variant regions from other studies: 136 SVs from 29 studies. See in: genome view
Overlapping variant regions from other studies: 29 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv512883 | Remapped | Pass | GRCh38.p12 | Primary Assembly | First Pass | NC_000006.12 | Chr6 | 64,386,529 | 64,388,912 |
| nsv512883 | Remapped | Pass | GRCh37.p13 | Primary Assembly | First Pass | NC_000006.11 | Chr6 | 65,096,422 | 65,098,805 |
| nsv512883 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000006.10 | Chr6 | 65,154,381 | 65,155,526 |
Variant Call Information
| Variant Call ID | Type | Sample ID | Method | Analysis | Other Calls in this Sample and Study |
|---|---|---|---|---|---|
| nssv625527 | insertion | 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 |
|---|---|---|---|---|---|---|---|---|---|
| nssv625527 | Remapped | Pass | NC_000006.12:g.(64 386529_?)_(?_64388 912)ins1224 | GRCh38.p12 | First Pass | NC_000006.12 | Chr6 | 64,386,529 | 64,388,912 |
| nssv625527 | Remapped | Pass | NC_000006.11:g.(65 096422_?)_(?_65098 805)ins1224 | GRCh37.p13 | First Pass | NC_000006.11 | Chr6 | 65,096,422 | 65,098,805 |
| nssv625527 | Submitted genomic | NC_000006.10:g.(65 154381_?)_(?_65155 526)ins1224 | NCBI36 (hg18) | NC_000006.10 | Chr6 | 65,154,381 | 65,155,526 |