nsv820355
- 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:59,501
- 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: 908 SVs from 89 studies. See in: genome view
Overlapping variant regions from other studies: 908 SVs from 89 studies. See in: genome view
Overlapping variant regions from other studies: 247 SVs from 28 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv820355 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000002.12 | Chr2 | 97,133,502 | 97,193,002 |
| nsv820355 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000002.11 | Chr2 | 97,799,239 | 97,858,739 |
| nsv820355 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000002.10 | Chr2 | 97,162,966 | 97,222,466 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv1420238 | Remapped | Perfect | NC_000002.12:g.(?_ 97133502)_(9719300 2_?)dup | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 97,133,502 | 97,193,002 |
| nssv1420238 | Remapped | Perfect | NC_000002.11:g.(?_ 97799239)_(9785873 9_?)dup | GRCh37.p13 | First Pass | NC_000002.11 | Chr2 | 97,799,239 | 97,858,739 |
| nssv1420238 | Submitted genomic | NC_000002.10:g.(?_ 97162966)_(9722246 6_?)dup | NCBI36 (hg18) | NC_000002.10 | Chr2 | 97,162,966 | 97,222,466 |