esv3978869
- Organism: Homo sapiens
- Study:estd229 (Fakhro et al. 2015)
- Variant Type:copy number variation
- Method Type:SNP array, Sequencing
- Submitted on:GRCh37 (hg19)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:145,901
- Publication(s):Fakhro et al. 2015
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: 675 SVs from 67 studies. See in: genome view
Overlapping variant regions from other studies: 675 SVs from 67 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Outer Start | Outer Stop |
|---|---|---|---|---|---|---|---|---|---|
| esv3978869 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000016.10 | Chr16 | 76,611,504 | 76,757,404 |
| esv3978869 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000016.9 | Chr16 | 76,645,401 | 76,791,301 |
Variant Call Information
| Variant Call ID | Type | Sample ID | Method | Analysis | Copy number | Other Calls in this Sample and Study |
|---|---|---|---|---|---|---|
| essv25974595 | duplication | DGMQ-31416 | SNP array, Sequencing | Other, Probe signal intensity, Read depth | 3 | 1,428 |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Outer Start | Outer Stop |
|---|---|---|---|---|---|---|---|---|---|
| essv25974595 | Remapped | Perfect | NC_000016.10:g.(76 611504_?)_(?_76757 404)dup | GRCh38.p12 | First Pass | NC_000016.10 | Chr16 | 76,611,504 | 76,757,404 |
| essv25974595 | Submitted genomic | NC_000016.9:g.(766 45401_?)_(?_767913 01)dup | GRCh37 (hg19) | NC_000016.9 | Chr16 | 76,645,401 | 76,791,301 |