nsv433401
- Organism: Homo sapiens
- Study:nstd14 (Cooper et al. 2008)
- Variant Type:copy number variation
- Method Type:SNP array
- Submitted on:NCBI35 (hg17)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:25,506
- Publication(s):Cooper 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: 265 SVs from 48 studies. See in: genome view
Overlapping variant regions from other studies: 265 SVs from 48 studies. See in: genome view
Overlapping variant regions from other studies: 4 SVs from 3 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv433401 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000008.11 | Chr8 | 56,158,777 | 56,184,282 |
| nsv433401 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000008.10 | Chr8 | 57,071,336 | 57,096,841 |
| nsv433401 | Submitted genomic | NCBI35 (hg17) | Primary Assembly | NC_000008.9 | Chr8 | 57,233,890 | 57,259,395 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv463282 | Remapped | Perfect | NC_000008.11:g.(?_ 56158777)_(5618428 2_?)dup | GRCh38.p12 | First Pass | NC_000008.11 | Chr8 | 56,158,777 | 56,184,282 |
| nssv463282 | Remapped | Perfect | NC_000008.10:g.(?_ 57071336)_(5709684 1_?)dup | GRCh37.p13 | First Pass | NC_000008.10 | Chr8 | 57,071,336 | 57,096,841 |
| nssv463282 | Submitted genomic | NC_000008.9:g.(?_5 7233890)_(57259395 _?)dup | NCBI35 (hg17) | NC_000008.9 | Chr8 | 57,233,890 | 57,259,395 |