esv3671448
- Organism: Homo sapiens
- Study:estd217 (Besenbacher et al. 2015)
- Variant Type:novel sequence insertion
- Method Type:Sequencing
- Submitted on:GRCh37 (hg19)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:1
- 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: 140 SVs from 26 studies. See in: genome view
Overlapping variant regions from other studies: 140 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 |
|---|---|---|---|---|---|---|---|---|---|
| esv3671448 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000004.12 | Chr4 | 144,474,093 | 144,474,093 |
| esv3671448 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000004.11 | Chr4 | 145,395,245 | 145,395,245 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis |
|---|---|---|---|
| essv16493506 | novel sequence insertion | Sequencing | de novo sequence assembly |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| essv16493506 | Remapped | Perfect | NC_000004.12:g.144 474093_144474094in s86 | GRCh38.p12 | First Pass | NC_000004.12 | Chr4 | 144,474,093 | 144,474,093 |
| essv16493506 | Submitted genomic | NC_000004.11:g.145 395245_145395246in s86 | GRCh37 (hg19) | NC_000004.11 | Chr4 | 145,395,245 | 145,395,245 |