nsv428279
- 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:325,367
- 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: 1231 SVs from 95 studies. See in: genome view
Overlapping variant regions from other studies: 1231 SVs from 95 studies. See in: genome view
Overlapping variant regions from other studies: 381 SVs from 30 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv428279 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000001.11 | Chr1 | 191,720,116 | 192,045,482 |
| nsv428279 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000001.10 | Chr1 | 191,689,246 | 192,014,612 |
| nsv428279 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000001.9 | Chr1 | 189,955,869 | 190,281,235 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv452587 | Remapped | Perfect | NC_000001.11:g.(?_ 191720116)_(192045 482_?)del | GRCh38.p12 | First Pass | NC_000001.11 | Chr1 | 191,720,116 | 192,045,482 |
| nssv452587 | Remapped | Perfect | NC_000001.10:g.(?_ 191689246)_(192014 612_?)del | GRCh37.p13 | First Pass | NC_000001.10 | Chr1 | 191,689,246 | 192,014,612 |
| nssv452587 | Submitted genomic | NC_000001.9:g.(?_1 89955869)_(1902812 35_?)del | NCBI36 (hg18) | NC_000001.9 | Chr1 | 189,955,869 | 190,281,235 |