nsv515232
- Organism: Homo sapiens
- Study:nstd46 (Campbell et al. 2011)
- Variant Type:copy number variation
- Method Type:Oligo aCGH
- Submitted on:NCBI36 (hg18)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:57,645
- Publication(s):Campbell et al. 2011
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: 545 SVs from 27 studies. See in: genome view
Overlapping variant regions from other studies: 546 SVs from 27 studies. See in: genome view
Overlapping variant regions from other studies: 154 SVs from 9 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv515232 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000024.10 | ChrY | 26,207,417 | 26,265,061 |
| nsv515232 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000024.9 | ChrY | 28,353,564 | 28,411,208 |
| nsv515232 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000024.8 | ChrY | 26,762,952 | 26,820,596 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv2995785 | Remapped | Perfect | NC_000024.10:g.(?_ 26207417)_(2626506 1_?)del | GRCh38.p12 | First Pass | NC_000024.10 | ChrY | 26,207,417 | 26,265,061 |
| nssv2995785 | Remapped | Perfect | NC_000024.9:g.(?_2 8353564)_(28411208 _?)del | GRCh37.p13 | First Pass | NC_000024.9 | ChrY | 28,353,564 | 28,411,208 |
| nssv2995785 | Submitted genomic | NC_000024.8:g.(?_2 6762952)_(26820596 _?)del | NCBI36 (hg18) | NC_000024.8 | ChrY | 26,762,952 | 26,820,596 |