esv1507318
- 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:18,522
- 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: 138 SVs from 32 studies. See in: genome view
Overlapping variant regions from other studies: 139 SVs from 32 studies. See in: genome view
Overlapping variant regions from other studies: 50 SVs from 14 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| esv1507318 | Remapped | Good | GRCh38.p12 | Primary Assembly | Second Pass | NC_000002.12 | Chr2 | 19,007,135 | 19,025,656 |
| esv1507318 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000002.11 | Chr2 | 19,195,287 | 19,213,771 |
| esv1507318 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000002.10 | Chr2 | 19,058,768 | 19,077,252 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| essv3930377 | Remapped | Good | NC_000002.12:g.190 07135_19025656del | GRCh38.p12 | Second Pass | NC_000002.12 | Chr2 | 19,007,135 | 19,025,656 |
| essv3930377 | Remapped | Perfect | NC_000002.11:g.191 95287_19213771del | GRCh37.p13 | First Pass | NC_000002.11 | Chr2 | 19,195,287 | 19,213,771 |
| essv3930377 | Submitted genomic | NC_000002.10:g.190 58768_19077252del | NCBI36 (hg18) | NC_000002.10 | Chr2 | 19,058,768 | 19,077,252 |