nsv984664
- 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:41,384,883
- 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: 119083 SVs from 145 studies. See in: genome view
Overlapping variant regions from other studies: 118817 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv984664 | Remapped | Good | GRCh38.p12 | Primary Assembly | First Pass | NC_000009.12 | Chr9 | 96,819,718 | 138,204,600 |
| nsv984664 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000009.11 | Chr9 | 99,582,000 | 141,095,050 |
Variant Call Information
| Variant Call ID | Type | Sample ID | Method | Analysis | Other Calls in this Sample and Study |
|---|---|---|---|---|---|
| nssv3217277 | complex substitution | ULSAM693 | SNP array | SNP genotyping analysis | nssv3217279 |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|
| nssv3217277 | Remapped | Good | GRCh38.p12 | First Pass | NC_000009.12 | Chr9 | 96,819,718 | 138,204,600 |
| nssv3217277 | Submitted genomic | GRCh37 (hg19) | NC_000009.11 | Chr9 | 99,582,000 | 141,095,050 |