nsv2732449
- Organism: Homo sapiens
- Study:nstd130 (Leppa et al. 2016)
- Variant Type:copy number variation
- Method Type:SNP array
- Submitted on:NCBI36 (hg18)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:16,829,801
- Publication(s):Leppa 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: 41140 SVs from 134 studies. See in: genome view
Overlapping variant regions from other studies: 41121 SVs from 134 studies. See in: genome view
Overlapping variant regions from other studies: 11716 SVs from 43 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv2732449 | Remapped | Good | GRCh38.p12 | Primary Assembly | First Pass | NC_000011.10 | Chr11 | 73,855,295 | 90,685,095 |
| nsv2732449 | Remapped | Good | GRCh37.p13 | Primary Assembly | First Pass | NC_000011.9 | Chr11 | 73,566,340 | 90,418,263 |
| nsv2732449 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000011.8 | Chr11 | 73,243,988 | 90,057,911 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis |
|---|---|---|---|
| nssv13592024 | duplication | SNP array | Probe signal intensity |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv13592024 | Remapped | Good | NC_000011.10:g.(?_ 73855295)_(9068509 5_?)dup | GRCh38.p12 | First Pass | NC_000011.10 | Chr11 | 73,855,295 | 90,685,095 |
| nssv13592024 | Remapped | Good | NC_000011.9:g.(?_7 3566340)_(90418263 _?)dup | GRCh37.p13 | First Pass | NC_000011.9 | Chr11 | 73,566,340 | 90,418,263 |
| nssv13592024 | Submitted genomic | NC_000011.8:g.(?_7 3243988)_(90057911 _?)dup | NCBI36 (hg18) | NC_000011.8 | Chr11 | 73,243,988 | 90,057,911 |