esv1010962
- Organism: Homo sapiens
- Study:estd180 (Pang et al. 2010)
- Variant Type:copy number variation
- Method Type:Oligo aCGH
- Submitted on:NCBI36 (hg18)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:35,873
- Publication(s):Pang et al. 2010
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: 209 SVs from 53 studies. See in: genome view
Overlapping variant regions from other studies: 215 SVs from 53 studies. See in: genome view
Overlapping variant regions from other studies: 81 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 | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| esv1010962 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000013.11 | Chr13 | 18,593,840 | 18,629,712 |
| esv1010962 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000013.10 | Chr13 | 19,167,980 | 19,203,852 |
| esv1010962 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000013.9 | Chr13 | 18,065,980 | 18,101,852 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| essv3586115 | Remapped | Perfect | NC_000013.11:g.(?_ 18593840)_(1862971 2_?)del | GRCh38.p12 | First Pass | NC_000013.11 | Chr13 | 18,593,840 | 18,629,712 |
| essv3586115 | Remapped | Perfect | NC_000013.10:g.(?_ 19167980)_(1920385 2_?)del | GRCh37.p13 | First Pass | NC_000013.10 | Chr13 | 19,167,980 | 19,203,852 |
| essv3586115 | Submitted genomic | NC_000013.9:g.(?_1 8065980)_(18101852 _?)del | NCBI36 (hg18) | NC_000013.9 | Chr13 | 18,065,980 | 18,101,852 |