nsv433377
- 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:27,535
- 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: 254 SVs from 52 studies. See in: genome view
Overlapping variant regions from other studies: 254 SVs from 52 studies. See in: genome view
Overlapping variant regions from other studies: 6 SVs from 5 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv433377 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000006.12 | Chr6 | 15,685,994 | 15,713,528 |
| nsv433377 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000006.11 | Chr6 | 15,686,225 | 15,713,759 |
| nsv433377 | Submitted genomic | NCBI35 (hg17) | Primary Assembly | NC_000006.9 | Chr6 | 15,794,204 | 15,821,738 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv463258 | Remapped | Perfect | NC_000006.12:g.(?_ 15685994)_(1571352 8_?)dup | GRCh38.p12 | First Pass | NC_000006.12 | Chr6 | 15,685,994 | 15,713,528 |
| nssv463258 | Remapped | Perfect | NC_000006.11:g.(?_ 15686225)_(1571375 9_?)dup | GRCh37.p13 | First Pass | NC_000006.11 | Chr6 | 15,686,225 | 15,713,759 |
| nssv463258 | Submitted genomic | NC_000006.9:g.(?_1 5794204)_(15821738 _?)dup | NCBI35 (hg17) | NC_000006.9 | Chr6 | 15,794,204 | 15,821,738 |