esv1333183
- Organism: Homo sapiens
- Study:estd22 (Levy et al. 2007)
- Variant Type:copy number variation
- Method Type:Sequencing
- Submitted on:NCBI36 (hg18)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:6,065
- 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: 177 SVs from 55 studies. See in: genome view
Overlapping variant regions from other studies: 177 SVs from 55 studies. See in: genome view
Overlapping variant regions from other studies: 47 SVs from 19 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| esv1333183 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000011.10 | Chr11 | 93,136,620 | 93,142,684 |
| esv1333183 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000011.9 | Chr11 | 92,869,786 | 92,875,850 |
| esv1333183 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000011.8 | Chr11 | 92,509,434 | 92,515,498 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| essv4163036 | Remapped | Perfect | NC_000011.10:g.931 36620_93142684del | GRCh38.p12 | First Pass | NC_000011.10 | Chr11 | 93,136,620 | 93,142,684 |
| essv4163036 | Remapped | Perfect | NC_000011.9:g.9286 9786_92875850del | GRCh37.p13 | First Pass | NC_000011.9 | Chr11 | 92,869,786 | 92,875,850 |
| essv4163036 | Submitted genomic | NC_000011.8:g.9250 9434_92515498del | NCBI36 (hg18) | NC_000011.8 | Chr11 | 92,509,434 | 92,515,498 |