nsv428284
- 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:175,141
- 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: 475 SVs from 55 studies. See in: genome view
Overlapping variant regions from other studies: 475 SVs from 55 studies. See in: genome view
Overlapping variant regions from other studies: 139 SVs from 13 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv428284 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000012.12 | Chr12 | 97,776,708 | 97,951,848 |
| nsv428284 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000012.11 | Chr12 | 98,170,486 | 98,345,626 |
| nsv428284 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000012.10 | Chr12 | 96,694,617 | 96,869,757 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv452311 | Remapped | Perfect | NC_000012.12:g.(?_ 97776708)_(9795184 8_?)dup | GRCh38.p12 | First Pass | NC_000012.12 | Chr12 | 97,776,708 | 97,951,848 |
| nssv452311 | Remapped | Perfect | NC_000012.11:g.(?_ 98170486)_(9834562 6_?)dup | GRCh37.p13 | First Pass | NC_000012.11 | Chr12 | 98,170,486 | 98,345,626 |
| nssv452311 | Submitted genomic | NC_000012.10:g.(?_ 96694617)_(9686975 7_?)dup | NCBI36 (hg18) | NC_000012.10 | Chr12 | 96,694,617 | 96,869,757 |