esv999382
- 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:44,304
- 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: 309 SVs from 58 studies. See in: genome view
Overlapping variant regions from other studies: 309 SVs from 58 studies. See in: genome view
Overlapping variant regions from other studies: 82 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 |
|---|---|---|---|---|---|---|---|---|---|
| esv999382 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000012.12 | Chr12 | 82,775,047 | 82,819,350 |
| esv999382 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000012.11 | Chr12 | 83,168,826 | 83,213,129 |
| esv999382 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000012.10 | Chr12 | 81,692,957 | 81,737,260 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| essv3586673 | Remapped | Perfect | NC_000012.12:g.(?_ 82775047)_(8281935 0_?)del | GRCh38.p12 | First Pass | NC_000012.12 | Chr12 | 82,775,047 | 82,819,350 |
| essv3586673 | Remapped | Perfect | NC_000012.11:g.(?_ 83168826)_(8321312 9_?)del | GRCh37.p13 | First Pass | NC_000012.11 | Chr12 | 83,168,826 | 83,213,129 |
| essv3586673 | Submitted genomic | NC_000012.10:g.(?_ 81692957)_(8173726 0_?)del | NCBI36 (hg18) | NC_000012.10 | Chr12 | 81,692,957 | 81,737,260 |