esv3675101
- Organism: Homo sapiens
- Study:estd217 (Besenbacher et al. 2015)
- Variant Type:sequence alteration
- Method Type:Sequencing
- Submitted on:GRCh37 (hg19)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:56
- Publication(s):Besenbacher 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: 153 SVs from 26 studies. See in: genome view
Overlapping variant regions from other studies: 153 SVs from 26 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| esv3675101 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000004.12 | Chr4 | 159,206,127 | 159,206,182 |
| esv3675101 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000004.11 | Chr4 | 160,127,279 | 160,127,334 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis |
|---|---|---|---|
| essv16496795 | sequence alteration | Sequencing | de novo sequence assembly |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|
| essv16496795 | Remapped | Perfect | GRCh38.p12 | First Pass | NC_000004.12 | Chr4 | 159,206,127 | 159,206,182 |
| essv16496795 | Submitted genomic | GRCh37 (hg19) | NC_000004.11 | Chr4 | 160,127,279 | 160,127,334 |