nsv820790
- 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:29,194
- 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: 176 SVs from 48 studies. See in: genome view
Overlapping variant regions from other studies: 176 SVs from 48 studies. See in: genome view
Overlapping variant regions from other studies: 62 SVs from 16 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv820790 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000019.10 | Chr19 | 8,272,250 | 8,301,443 |
| nsv820790 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000019.9 | Chr19 | 8,337,134 | 8,366,327 |
| nsv820790 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000019.8 | Chr19 | 8,243,134 | 8,272,327 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv1420035 | Remapped | Perfect | NC_000019.10:g.(?_ 8272250)_(8301443_ ?)del | GRCh38.p12 | First Pass | NC_000019.10 | Chr19 | 8,272,250 | 8,301,443 |
| nssv1420035 | Remapped | Perfect | NC_000019.9:g.(?_8 337134)_(8366327_? )del | GRCh37.p13 | First Pass | NC_000019.9 | Chr19 | 8,337,134 | 8,366,327 |
| nssv1420035 | Submitted genomic | NC_000019.8:g.(?_8 243134)_(8272327_? )del | NCBI36 (hg18) | NC_000019.8 | Chr19 | 8,243,134 | 8,272,327 |