esv998961
- Organism: Homo sapiens
- Study:estd180 (Pang et al. 2010)
- Variant Type:copy number variation
- Method Type:Oligo aCGH
- Submitted on:NCBI36 (hg18)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:160,788
- Publication(s):Pang et al. 2010
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: 4184 SVs from 97 studies. See in: genome view
Overlapping variant regions from other studies: 4177 SVs from 97 studies. See in: genome view
Overlapping variant regions from other studies: 2917 SVs from 36 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 |
|---|---|---|---|---|---|---|---|---|---|
| esv998961 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000015.10 | Chr15 | 20,344,141 | 20,504,928 |
| esv998961 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000015.9 | Chr15 | 20,549,394 | 20,710,181 |
| esv998961 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000015.8 | Chr15 | 18,809,408 | 18,970,195 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| essv3586355 | Remapped | Perfect | NC_000015.10:g.(?_ 20344141)_(2050492 8_?)del | GRCh38.p12 | First Pass | NC_000015.10 | Chr15 | 20,344,141 | 20,504,928 |
| essv3586355 | Remapped | Perfect | NC_000015.9:g.(?_2 0549394)_(20710181 _?)del | GRCh37.p13 | First Pass | NC_000015.9 | Chr15 | 20,549,394 | 20,710,181 |
| essv3586355 | Submitted genomic | NC_000015.8:g.(?_1 8809408)_(18970195 _?)del | NCBI36 (hg18) | NC_000015.8 | Chr15 | 18,809,408 | 18,970,195 |