esv1091832
- Organism: Homo sapiens
- Study:estd22 (Levy et al. 2007)
- Variant Type:copy number variation
- Method Type:Sequencing
- Submitted on:NCBI36 (hg18)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:3
- Publication(s):Levy et al. 2007
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: 105 SVs from 16 studies. See in: genome view
Overlapping variant regions from other studies: 105 SVs from 16 studies. See in: genome view
Overlapping variant regions from other studies: 21 SVs from 7 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| esv1091832 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000017.11 | Chr17 | 68,489,356 | 68,489,358 |
| esv1091832 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000017.10 | Chr17 | 66,485,497 | 66,485,499 |
| esv1091832 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000017.9 | Chr17 | 63,997,092 | 63,997,094 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| essv3638792 | Remapped | Perfect | NC_000017.11:g.684 89356_68489358del | GRCh38.p12 | First Pass | NC_000017.11 | Chr17 | 68,489,356 | 68,489,358 |
| essv3638792 | Remapped | Perfect | NC_000017.10:g.664 85497_66485499del | GRCh37.p13 | First Pass | NC_000017.10 | Chr17 | 66,485,497 | 66,485,499 |
| essv3638792 | Submitted genomic | NC_000017.9:g.6399 7092_63997094del | NCBI36 (hg18) | NC_000017.9 | Chr17 | 63,997,092 | 63,997,094 |