esv1000327
- 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:56,942
- 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: 798 SVs from 75 studies. See in: genome view
Overlapping variant regions from other studies: 798 SVs from 75 studies. See in: genome view
Overlapping variant regions from other studies: 265 SVs from 19 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 |
|---|---|---|---|---|---|---|---|---|---|
| esv1000327 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000004.12 | Chr4 | 10,133,980 | 10,190,921 |
| esv1000327 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000004.11 | Chr4 | 10,135,604 | 10,192,545 |
| esv1000327 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000004.10 | Chr4 | 9,744,702 | 9,801,643 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| essv3586269 | Remapped | Perfect | NC_000004.12:g.(?_ 10133980)_(1019092 1_?)dup | GRCh38.p12 | First Pass | NC_000004.12 | Chr4 | 10,133,980 | 10,190,921 |
| essv3586269 | Remapped | Perfect | NC_000004.11:g.(?_ 10135604)_(1019254 5_?)dup | GRCh37.p13 | First Pass | NC_000004.11 | Chr4 | 10,135,604 | 10,192,545 |
| essv3586269 | Submitted genomic | NC_000004.10:g.(?_ 9744702)_(9801643_ ?)dup | NCBI36 (hg18) | NC_000004.10 | Chr4 | 9,744,702 | 9,801,643 |