esv29610
- Organism: Homo sapiens
- Study:estd20 (Conrad et al. 2009)
- Variant Type:sequence alteration
- Method Type:Oligo aCGH
- Submitted on:NCBI36 (hg18)
- Variant Calls:2
- Validation:Not tested
- Clinical Assertions: No
- Region Size:90,956
- 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: 656 SVs from 72 studies. See in: genome view
Overlapping variant regions from other studies: 643 SVs from 68 studies. See in: genome view
Overlapping variant regions from other studies: 149 SVs from 22 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 |
|---|---|---|---|---|---|---|---|---|---|
| esv29610 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000020.11 | Chr20 | 30,185,378 | 30,276,333 |
| esv29610 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000020.10 | Chr20 | 29,420,054 | 29,511,009 |
| esv29610 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000020.9 | Chr20 | 28,033,715 | 28,124,670 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|
| esv17005 | Remapped | Perfect | GRCh38.p12 | First Pass | NC_000020.11 | Chr20 | 30,185,378 | 30,275,718 |
| esv10166 | Remapped | Perfect | GRCh38.p12 | First Pass | NC_000020.11 | Chr20 | 30,272,223 | 30,276,333 |
| esv17005 | Remapped | Perfect | GRCh37.p13 | First Pass | NC_000020.10 | Chr20 | 29,420,054 | 29,510,394 |
| esv10166 | Remapped | Perfect | GRCh37.p13 | First Pass | NC_000020.10 | Chr20 | 29,506,899 | 29,511,009 |
| esv17005 | Submitted genomic | NCBI36 (hg18) | NC_000020.9 | Chr20 | 28,033,715 | 28,124,055 | ||
| esv10166 | Submitted genomic | NCBI36 (hg18) | NC_000020.9 | Chr20 | 28,120,560 | 28,124,670 |