esv1827418
- Organism: Homo sapiens
- Study:estd188 (Pinto et al. 2011)
- Variant Type:copy number variation
- Method Type:Oligo aCGH
- Submitted on:NCBI36 (hg18)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:213,431
- Publication(s):Pinto et al. 2011
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: 427 SVs from 57 studies. See in: genome view
Overlapping variant regions from other studies: 174 SVs from 30 studies. See in: genome view
Overlapping variant regions from other studies: 65 SVs from 17 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 |
|---|---|---|---|---|---|---|---|---|---|
| esv1827418 | Remapped | Pass | GRCh38.p12 | Primary Assembly | First Pass | NC_000011.10 | Chr11 | 70,952,104 | 71,165,534 |
| esv1827418 | Remapped | Pass | GRCh37.p13 | PATCHES | First Pass | NW_004070871.1 | Chr11|NW_0 04070871.1 | 591,000 | 659,747 |
| esv1827418 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000011.8 | Chr11 | 70,475,896 | 70,554,228 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| essv4368700 | Remapped | Pass | NC_000011.10:g.(?_ 70952104)_(7116553 4_?)del | GRCh38.p12 | First Pass | NC_000011.10 | Chr11 | 70,952,104 | 71,165,534 |
| essv4368700 | Remapped | Pass | NW_004070871.1:g.( ?_591000)_(659747_ ?)del | GRCh37.p13 | First Pass | NW_004070871.1 | Chr11|NW_0 04070871.1 | 591,000 | 659,747 |
| essv4368700 | Submitted genomic | NC_000011.8:g.(?_7 0475896)_(70554228 _?)del | NCBI36 (hg18) | NC_000011.8 | Chr11 | 70,475,896 | 70,554,228 |