esv29057
- Organism: Homo sapiens
- Study:estd20 (Conrad et al. 2009)
- Variant Type:sequence alteration
- Method Type:Oligo aCGH
- Submitted on:NCBI36 (hg18)
- Variant Calls:3
- Validation:Not tested
- Clinical Assertions: No
- Region Size:8,638
- Publication(s):Conrad et al. 2009
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: 216 SVs from 29 studies. See in: genome view
Overlapping variant regions from other studies: 216 SVs from 29 studies. See in: genome view
Overlapping variant regions from other studies: 130 SVs from 13 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 |
|---|---|---|---|---|---|---|---|---|---|
| esv29057 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000006.12 | Chr6 | 3,253,683 | 3,262,320 |
| esv29057 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000006.11 | Chr6 | 3,253,917 | 3,262,554 |
| esv29057 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000006.10 | Chr6 | 3,198,916 | 3,207,553 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|
| esv20906 | Remapped | Perfect | GRCh38.p12 | First Pass | NC_000006.12 | Chr6 | 3,253,683 | 3,262,320 |
| esv14983 | Remapped | Perfect | GRCh38.p12 | First Pass | NC_000006.12 | Chr6 | 3,254,219 | 3,255,959 |
| esv17107 | Remapped | Perfect | GRCh38.p12 | First Pass | NC_000006.12 | Chr6 | 3,255,473 | 3,255,959 |
| esv20906 | Remapped | Perfect | GRCh37.p13 | First Pass | NC_000006.11 | Chr6 | 3,253,917 | 3,262,554 |
| esv14983 | Remapped | Perfect | GRCh37.p13 | First Pass | NC_000006.11 | Chr6 | 3,254,453 | 3,256,193 |
| esv17107 | Remapped | Perfect | GRCh37.p13 | First Pass | NC_000006.11 | Chr6 | 3,255,707 | 3,256,193 |
| esv20906 | Submitted genomic | NCBI36 (hg18) | NC_000006.10 | Chr6 | 3,198,916 | 3,207,553 | ||
| esv14983 | Submitted genomic | NCBI36 (hg18) | NC_000006.10 | Chr6 | 3,199,452 | 3,201,192 | ||
| esv17107 | Submitted genomic | NCBI36 (hg18) | NC_000006.10 | Chr6 | 3,200,706 | 3,201,192 |