esv1592514
- 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:4
- 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: 190 SVs from 31 studies. See in: genome view
Overlapping variant regions from other studies: 190 SVs from 31 studies. See in: genome view
Overlapping variant regions from other studies: 96 SVs from 11 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| esv1592514 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000013.11 | Chr13 | 20,050,517 | 20,050,520 |
| esv1592514 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000013.10 | Chr13 | 20,624,657 | 20,624,660 |
| esv1592514 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000013.9 | Chr13 | 19,522,657 | 19,522,660 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| essv3632760 | Remapped | Perfect | NC_000013.11:g.200 50517_20050520del | GRCh38.p12 | First Pass | NC_000013.11 | Chr13 | 20,050,517 | 20,050,520 |
| essv3632760 | Remapped | Perfect | NC_000013.10:g.206 24657_20624660del | GRCh37.p13 | First Pass | NC_000013.10 | Chr13 | 20,624,657 | 20,624,660 |
| essv3632760 | Submitted genomic | NC_000013.9:g.1952 2657_19522660del | NCBI36 (hg18) | NC_000013.9 | Chr13 | 19,522,657 | 19,522,660 |