nsv817609
- Organism: Homo sapiens
- Study:nstd58 (Forsberg et al. 2012)
- Variant Type:complex substitution
- Method Type:SNP array
- Submitted on:NCBI36 (hg18)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:76,744,335
- Publication(s):Forsberg et al. 2012
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: 200129 SVs from 147 studies. See in: genome view
Overlapping variant regions from other studies: 199724 SVs from 147 studies. See in: genome view
Overlapping variant regions from other studies: 59231 SVs from 44 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Outer Start | Inner Start | Inner Stop | Outer Stop |
|---|---|---|---|---|---|---|---|---|---|---|---|
| nsv817609 | Remapped | Good | GRCh38.p12 | Primary Assembly | First Pass | NC_000010.11 | Chr10 | 57,042,662 | 57,042,662 | 133,786,996 | 133,786,996 |
| nsv817609 | Remapped | Good | GRCh37.p13 | Primary Assembly | First Pass | NC_000010.10 | Chr10 | 58,802,422 | 58,802,422 | 135,524,321 | 135,524,321 |
| nsv817609 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000010.9 | Chr10 | 58,472,428 | 58,880,087 | 135,374,311 | 135,374,311 |
Variant Call Information
| Variant Call ID | Type | Sample ID | Method | Analysis |
|---|---|---|---|---|
| nssv1415553 | complex substitution | TP12-2 | SNP array | SNP genotyping analysis |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | Assembly | Reciprocity | Sequence ID | Chr | Outer Start | Inner Start | Inner Stop | Outer Stop |
|---|---|---|---|---|---|---|---|---|---|---|
| nssv1415553 | Remapped | Good | GRCh38.p12 | First Pass | NC_000010.11 | Chr10 | 57,042,662 | 57,042,662 | 133,786,996 | 133,786,996 |
| nssv1415553 | Remapped | Good | GRCh37.p13 | First Pass | NC_000010.10 | Chr10 | 58,802,422 | 58,802,422 | 135,524,321 | 135,524,321 |
| nssv1415553 | Submitted genomic | NCBI36 (hg18) | NC_000010.9 | Chr10 | 58,472,428 | 58,880,087 | 135,374,311 | 135,374,311 |