nsv428170
- 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:134,106
- 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: 613 SVs from 67 studies. See in: genome view
Overlapping variant regions from other studies: 599 SVs from 67 studies. See in: genome view
Overlapping variant regions from other studies: 198 SVs from 21 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv428170 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000007.14 | Chr7 | 72,318,449 | 72,452,554 |
| nsv428170 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000007.13 | Chr7 | 71,783,434 | 71,917,539 |
| nsv428170 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000007.12 | Chr7 | 71,421,370 | 71,555,475 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv451056 | Remapped | Perfect | NC_000007.14:g.(?_ 72318449)_(7245255 4_?)del | GRCh38.p12 | First Pass | NC_000007.14 | Chr7 | 72,318,449 | 72,452,554 |
| nssv451056 | Remapped | Perfect | NC_000007.13:g.(?_ 71783434)_(7191753 9_?)del | GRCh37.p13 | First Pass | NC_000007.13 | Chr7 | 71,783,434 | 71,917,539 |
| nssv451056 | Submitted genomic | NC_000007.12:g.(?_ 71421370)_(7155547 5_?)del | NCBI36 (hg18) | NC_000007.12 | Chr7 | 71,421,370 | 71,555,475 |