nsv431186
- Organism: Homo sapiens
- Study:nstd12 (Marshall et al. 2008)
- Variant Type:complex substitution
- Method Type:Merging, SNP array
- Submitted on:NCBI35 (hg17)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:2,338,233
- Publication(s):Marshall et al. 2008
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: 13876 SVs from 121 studies. See in: genome view
Overlapping variant regions from other studies: 13835 SVs from 124 studies. See in: genome view
Overlapping variant regions from other studies: 693 SVs from 17 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv431186 | Remapped | Pass | GRCh38.p12 | Primary Assembly | First Pass | NC_000015.10 | Chr15 | 19,961,836 | 22,300,068 |
| nsv431186 | Remapped | Pass | GRCh37.p13 | Primary Assembly | First Pass | NC_000015.9 | Chr15 | 20,167,089 | 22,588,019 |
| nsv431186 | Submitted genomic | NCBI35 (hg17) | Primary Assembly | NC_000015.8 | Chr15 | 18,427,103 | 20,089,383 |
Variant Call Information
| Variant Call ID | Type | Sample ID | Method | Analysis | Other Calls in this Sample and Study |
|---|---|---|---|---|---|
| nssv563176 | complex substitution | 82058L | Merging, SNP array | Merging, SNP genotyping analysis | 16 |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|
| nssv563176 | Remapped | Pass | GRCh38.p12 | First Pass | NC_000015.10 | Chr15 | 19,961,836 | 22,300,068 |
| nssv563176 | Remapped | Pass | GRCh37.p13 | First Pass | NC_000015.9 | Chr15 | 20,167,089 | 22,588,019 |
| nssv563176 | Submitted genomic | NCBI35 (hg17) | NC_000015.8 | Chr15 | 18,427,103 | 20,089,383 |