esv1309138
- 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:13
- 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: 187 SVs from 29 studies. See in: genome view
Overlapping variant regions from other studies: 187 SVs from 29 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 |
|---|---|---|---|---|---|---|---|---|---|
| esv1309138 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000013.11 | Chr13 | 20,046,627 | 20,046,639 |
| esv1309138 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000013.10 | Chr13 | 20,620,767 | 20,620,779 |
| esv1309138 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000013.9 | Chr13 | 19,518,767 | 19,518,779 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| essv3678485 | Remapped | Perfect | NC_000013.11:g.200 46627_20046639del | GRCh38.p12 | First Pass | NC_000013.11 | Chr13 | 20,046,627 | 20,046,639 |
| essv3678485 | Remapped | Perfect | NC_000013.10:g.206 20767_20620779del | GRCh37.p13 | First Pass | NC_000013.10 | Chr13 | 20,620,767 | 20,620,779 |
| essv3678485 | Submitted genomic | NC_000013.9:g.1951 8767_19518779del | NCBI36 (hg18) | NC_000013.9 | Chr13 | 19,518,767 | 19,518,779 |