nsv428278
- Organism: Homo sapiens
- Study:nstd8 (Perry et al. 2008b)
- Variant Type:copy number variation
- Method Type:BAC aCGH
- Submitted on:NCBI36 (hg18)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:296,735
- Publication(s):Perry 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: 2590 SVs from 83 studies. See in: genome view
Overlapping variant regions from other studies: 2590 SVs from 83 studies. See in: genome view
Overlapping variant regions from other studies: 1073 SVs from 25 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv428278 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000012.12 | Chr12 | 37,462,893 | 37,759,627 |
| nsv428278 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000012.11 | Chr12 | 37,856,695 | 38,153,429 |
| nsv428278 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000012.10 | Chr12 | 36,142,962 | 36,439,696 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv452284 | Remapped | Perfect | NC_000012.12:g.(?_ 37462893)_(3775962 7_?)dup | GRCh38.p12 | First Pass | NC_000012.12 | Chr12 | 37,462,893 | 37,759,627 |
| nssv452284 | Remapped | Perfect | NC_000012.11:g.(?_ 37856695)_(3815342 9_?)dup | GRCh37.p13 | First Pass | NC_000012.11 | Chr12 | 37,856,695 | 38,153,429 |
| nssv452284 | Submitted genomic | NC_000012.10:g.(?_ 36142962)_(3643969 6_?)dup | NCBI36 (hg18) | NC_000012.10 | Chr12 | 36,142,962 | 36,439,696 |