nsv984745
- Organism: Homo sapiens
- Study:nstd92 (Forsberg et al. 2014)
- Variant Type:complex substitution
- Method Type:SNP array
- Submitted on:GRCh37 (hg19)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:81,655,995
- Publication(s):Forsberg et al. 2014
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: 217277 SVs from 145 studies. See in: genome view
Overlapping variant regions from other studies: 217085 SVs from 145 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nsv984745 | Remapped | Good | GRCh38.p12 | Primary Assembly | First Pass | NC_000012.12 | Chr12 | 51,546,216 | 133,202,210 |
| nsv984745 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000012.11 | Chr12 | 51,940,000 | 133,778,796 |
Variant Call Information
| Variant Call ID | Type | Sample ID | Method | Analysis |
|---|---|---|---|---|
| nssv3217392 | complex substitution | PIVUS510 | SNP array | SNP genotyping analysis |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|
| nssv3217392 | Remapped | Good | GRCh38.p12 | First Pass | NC_000012.12 | Chr12 | 51,546,216 | 133,202,210 |
| nssv3217392 | Submitted genomic | GRCh37 (hg19) | NC_000012.11 | Chr12 | 51,940,000 | 133,778,796 |