esv1035653
- 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:2
- 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 17 studies. See in: genome view
Overlapping variant regions from other studies: 105 SVs from 17 studies. See in: genome view
Overlapping variant regions from other studies: 20 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 |
|---|---|---|---|---|---|---|---|---|---|
| esv1035653 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000017.11 | Chr17 | 68,511,669 | 68,511,670 |
| esv1035653 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000017.10 | Chr17 | 66,507,810 | 66,507,811 |
| esv1035653 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000017.9 | Chr17 | 64,019,405 | 64,019,406 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| essv3827383 | Remapped | Perfect | NC_000017.11:g.685 11669_68511670del | GRCh38.p12 | First Pass | NC_000017.11 | Chr17 | 68,511,669 | 68,511,670 |
| essv3827383 | Remapped | Perfect | NC_000017.10:g.665 07810_66507811del | GRCh37.p13 | First Pass | NC_000017.10 | Chr17 | 66,507,810 | 66,507,811 |
| essv3827383 | Submitted genomic | NC_000017.9:g.6401 9405_64019406del | NCBI36 (hg18) | NC_000017.9 | Chr17 | 64,019,405 | 64,019,406 |