nsv2768225
- Organism: Homo sapiens
- Study:nstd125 (Wills et al. 2016)
- Variant Type:complex substitution
- Method Type:SNP array
- Submitted on:GRCh37 (hg19)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:159,043,305
- Description:mosaic
- Publication(s):Wills et al. 2016
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: 449746 SVs from 156 studies. See in: genome view
Overlapping variant regions from other studies: 447988 SVs from 156 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv2768225 | Remapped | Good | GRCh38.p12 | Primary Assembly | First Pass | NC_000007.14 | Chr7 | 242,519 | 159,285,823 |
| nsv2768225 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000007.13 | Chr7 | 260,911 | 159,078,512 |
Variant Call Information
| Variant Call ID | Type | Sample ID | Method | Analysis | Copy number | Other Calls in this Sample and Study |
|---|---|---|---|---|---|---|
| nssv13638290 | complex substitution | 12 | SNP array | SNP genotyping analysis | 3 | nssv13638291, nssv13638292 |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|
| nssv13638290 | Remapped | Good | GRCh38.p12 | First Pass | NC_000007.14 | Chr7 | 242,519 | 159,285,823 |
| nssv13638290 | Submitted genomic | GRCh37 (hg19) | NC_000007.13 | Chr7 | 260,911 | 159,078,512 |