esv3656885
- Organism: Homo sapiens
- Study:estd217 (Besenbacher et al. 2015)
- Variant Type:complex substitution
- Method Type:Sequencing
- Submitted on:GRCh37 (hg19)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:2,530
- 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: 260 SVs from 53 studies. See in: genome view
Overlapping variant regions from other studies: 260 SVs from 53 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| esv3656885 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000009.12 | Chr9 | 76,304,559 | 76,307,088 |
| esv3656885 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000009.11 | Chr9 | 78,919,475 | 78,922,004 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis |
|---|---|---|---|
| essv16463472 | complex substitution | Sequencing | de novo sequence assembly |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|
| essv16463472 | Remapped | Perfect | GRCh38.p12 | First Pass | NC_000009.12 | Chr9 | 76,304,559 | 76,307,088 |
| essv16463472 | Submitted genomic | GRCh37 (hg19) | NC_000009.11 | Chr9 | 78,919,475 | 78,922,004 |