nsv826688
- Organism: Homo sapiens
- Study:nstd67 (Park et al. 2010)
- Variant Type:copy number variation
- Method Type:Oligo aCGH
- Submitted on:NCBI36 (hg18)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:89,786
- Publication(s):Park et al. 2010
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: 498 SVs from 49 studies. See in: genome view
Overlapping variant regions from other studies: 498 SVs from 49 studies. See in: genome view
Overlapping variant regions from other studies: 193 SVs from 19 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv826688 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000013.11 | Chr13 | 66,654,883 | 66,744,668 |
| nsv826688 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000013.10 | Chr13 | 67,229,015 | 67,318,800 |
| nsv826688 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000013.9 | Chr13 | 66,127,016 | 66,216,801 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv1435641 | Remapped | Perfect | NC_000013.11:g.(?_ 66654883)_(6674466 8_?)del | GRCh38.p12 | First Pass | NC_000013.11 | Chr13 | 66,654,883 | 66,744,668 |
| nssv1435641 | Remapped | Perfect | NC_000013.10:g.(?_ 67229015)_(6731880 0_?)del | GRCh37.p13 | First Pass | NC_000013.10 | Chr13 | 67,229,015 | 67,318,800 |
| nssv1435641 | Submitted genomic | NC_000013.9:g.(?_6 6127016)_(66216801 _?)del | NCBI36 (hg18) | NC_000013.9 | Chr13 | 66,127,016 | 66,216,801 |