esv1585596
- 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:6,052
- 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: 198 SVs from 54 studies. See in: genome view
Overlapping variant regions from other studies: 198 SVs from 54 studies. See in: genome view
Overlapping variant regions from other studies: 71 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 | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| esv1585596 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000004.12 | Chr4 | 93,638,303 | 93,644,354 |
| esv1585596 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000004.11 | Chr4 | 94,559,454 | 94,565,505 |
| esv1585596 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000004.10 | Chr4 | 94,778,477 | 94,784,528 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| essv4015401 | Remapped | Perfect | NC_000004.12:g.936 38303_93644354del | GRCh38.p12 | First Pass | NC_000004.12 | Chr4 | 93,638,303 | 93,644,354 |
| essv4015401 | Remapped | Perfect | NC_000004.11:g.945 59454_94565505del | GRCh37.p13 | First Pass | NC_000004.11 | Chr4 | 94,559,454 | 94,565,505 |
| essv4015401 | Submitted genomic | NC_000004.10:g.947 78477_94784528del | NCBI36 (hg18) | NC_000004.10 | Chr4 | 94,778,477 | 94,784,528 |