esv988673
- Organism: Homo sapiens
- Study:estd180 (Pang et al. 2010)
- Variant Type:copy number variation
- Method Type:Sequencing
- Submitted on:NCBI36 (hg18)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:15
- 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: 136 SVs from 21 studies. See in: genome view
Overlapping variant regions from other studies: 136 SVs from 21 studies. See in: genome view
Overlapping variant regions from other studies: 32 SVs from 8 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| esv988673 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000017.11 | Chr17 | 65,848,860 | 65,848,874 |
| esv988673 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000017.10 | Chr17 | 63,844,978 | 63,844,992 |
| esv988673 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000017.9 | Chr17 | 61,275,440 | 61,275,454 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| essv3584957 | Remapped | Perfect | NC_000017.11:g.658 48860_65848874del1 5 | GRCh38.p12 | First Pass | NC_000017.11 | Chr17 | 65,848,860 | 65,848,874 |
| essv3584957 | Remapped | Perfect | NC_000017.10:g.638 44978_63844992del1 5 | GRCh37.p13 | First Pass | NC_000017.10 | Chr17 | 63,844,978 | 63,844,992 |
| essv3584957 | Submitted genomic | NC_000017.9:g.6127 5440_61275454del15 | NCBI36 (hg18) | NC_000017.9 | Chr17 | 61,275,440 | 61,275,454 |