nsv821368
- Organism: Homo sapiens
- Study:nstd65 (Ju et al. 2010)
- Variant Type:copy number variation
- Method Type:Sequencing
- Submitted on:NCBI36 (hg18)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:16,168
- Publication(s):Ju 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: 853 SVs from 91 studies. See in: genome view
Overlapping variant regions from other studies: 853 SVs from 91 studies. See in: genome view
Overlapping variant regions from other studies: 408 SVs from 29 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv821368 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000011.10 | Chr11 | 18,927,654 | 18,943,821 |
| nsv821368 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000011.9 | Chr11 | 18,949,201 | 18,965,368 |
| nsv821368 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000011.8 | Chr11 | 18,905,777 | 18,921,944 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv1420930 | Remapped | Perfect | NC_000011.10:g.(?_ 18927654)_(1894382 1_?)del | GRCh38.p12 | First Pass | NC_000011.10 | Chr11 | 18,927,654 | 18,943,821 |
| nssv1420930 | Remapped | Perfect | NC_000011.9:g.(?_1 8949201)_(18965368 _?)del | GRCh37.p13 | First Pass | NC_000011.9 | Chr11 | 18,949,201 | 18,965,368 |
| nssv1420930 | Submitted genomic | NC_000011.8:g.(?_1 8905777)_(18921944 _?)del | NCBI36 (hg18) | NC_000011.8 | Chr11 | 18,905,777 | 18,921,944 |