nsv428136
- 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:185,602
- 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: 642 SVs from 65 studies. See in: genome view
Overlapping variant regions from other studies: 642 SVs from 65 studies. See in: genome view
Overlapping variant regions from other studies: 155 SVs from 15 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv428136 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000006.12 | Chr6 | 15,595,409 | 15,781,010 |
| nsv428136 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000006.11 | Chr6 | 15,595,640 | 15,781,241 |
| nsv428136 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000006.10 | Chr6 | 15,703,619 | 15,889,220 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv450608 | Remapped | Perfect | NC_000006.12:g.(?_ 15595409)_(1578101 0_?)dup | GRCh38.p12 | First Pass | NC_000006.12 | Chr6 | 15,595,409 | 15,781,010 |
| nssv450608 | Remapped | Perfect | NC_000006.11:g.(?_ 15595640)_(1578124 1_?)dup | GRCh37.p13 | First Pass | NC_000006.11 | Chr6 | 15,595,640 | 15,781,241 |
| nssv450608 | Submitted genomic | NC_000006.10:g.(?_ 15703619)_(1588922 0_?)dup | NCBI36 (hg18) | NC_000006.10 | Chr6 | 15,703,619 | 15,889,220 |