nsv433411
- 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:95,428
- 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: 425 SVs from 59 studies. See in: genome view
Overlapping variant regions from other studies: 419 SVs from 58 studies. See in: genome view
Overlapping variant regions from other studies: 23 SVs from 6 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv433411 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000010.11 | Chr10 | 42,362,706 | 42,458,133 |
| nsv433411 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000010.10 | Chr10 | 42,858,154 | 42,953,581 |
| nsv433411 | Submitted genomic | NCBI35 (hg17) | Primary Assembly | NC_000010.8 | Chr10 | 42,178,160 | 42,273,587 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv463292 | Remapped | Perfect | NC_000010.11:g.(?_ 42362706)_(4245813 3_?)dup | GRCh38.p12 | First Pass | NC_000010.11 | Chr10 | 42,362,706 | 42,458,133 |
| nssv463292 | Remapped | Perfect | NC_000010.10:g.(?_ 42858154)_(4295358 1_?)dup | GRCh37.p13 | First Pass | NC_000010.10 | Chr10 | 42,858,154 | 42,953,581 |
| nssv463292 | Submitted genomic | NC_000010.8:g.(?_4 2178160)_(42273587 _?)dup | NCBI35 (hg17) | NC_000010.8 | Chr10 | 42,178,160 | 42,273,587 |