esv29969
- Organism: Homo sapiens
- Study:estd22 (Levy et al. 2007)
- Variant Type:copy number variation
- Method Type:Oligo aCGH, SNP array
- Submitted on:NCBI36 (hg18)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:159,004
- 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: 2581 SVs from 94 studies. See in: genome view
Overlapping variant regions from other studies: 2581 SVs from 94 studies. See in: genome view
Overlapping variant regions from other studies: 636 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 |
|---|---|---|---|---|---|---|---|---|---|
| esv29969 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000020.11 | Chr20 | 14,801,038 | 14,960,041 |
| esv29969 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000020.10 | Chr20 | 14,781,684 | 14,940,687 |
| esv29969 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000020.9 | Chr20 | 14,729,684 | 14,888,687 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| essv84208 | Remapped | Perfect | NC_000020.11:g.(?_ 14801038)_(1496004 1_?)dup | GRCh38.p12 | First Pass | NC_000020.11 | Chr20 | 14,801,038 | 14,960,041 |
| essv84208 | Remapped | Perfect | NC_000020.10:g.(?_ 14781684)_(1494068 7_?)dup | GRCh37.p13 | First Pass | NC_000020.10 | Chr20 | 14,781,684 | 14,940,687 |
| essv84208 | Submitted genomic | NC_000020.9:g.(?_1 4729684)_(14888687 _?)dup | NCBI36 (hg18) | NC_000020.9 | Chr20 | 14,729,684 | 14,888,687 |