esv1007713
- Organism: Homo sapiens
- Study:estd180 (Pang et al. 2010)
- Variant Type:copy number variation
- Method Type:SNP array
- Submitted on:NCBI36 (hg18)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:38,671
- Publication(s):Pang 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: 706 SVs from 74 studies. See in: genome view
Overlapping variant regions from other studies: 709 SVs from 74 studies. See in: genome view
Overlapping variant regions from other studies: 293 SVs from 26 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 |
|---|---|---|---|---|---|---|---|---|---|
| esv1007713 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000001.11 | Chr1 | 169,245,563 | 169,284,233 |
| esv1007713 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000001.10 | Chr1 | 169,214,801 | 169,253,471 |
| esv1007713 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000001.9 | Chr1 | 167,481,425 | 167,520,095 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| essv3586048 | Remapped | Perfect | NC_000001.11:g.(?_ 169245563)_(169284 233_?)del | GRCh38.p12 | First Pass | NC_000001.11 | Chr1 | 169,245,563 | 169,284,233 |
| essv3586048 | Remapped | Perfect | NC_000001.10:g.(?_ 169214801)_(169253 471_?)del | GRCh37.p13 | First Pass | NC_000001.10 | Chr1 | 169,214,801 | 169,253,471 |
| essv3586048 | Submitted genomic | NC_000001.9:g.(?_1 67481425)_(1675200 95_?)del | NCBI36 (hg18) | NC_000001.9 | Chr1 | 167,481,425 | 167,520,095 |