esv2881906
- Organism: Homo sapiens
- Study:estd209 (Pang et al. 2014b)
- Variant Type:insertion
- Method Type:Sequencing
- Submitted on:GRCh37 (hg19)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:35
- Publication(s):Pang et al. 2014
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: 98 SVs from 22 studies. See in: genome view
Overlapping variant regions from other studies: 98 SVs from 22 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| esv2881906 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000010.11 | Chr10 | 102,528,986 | 102,529,020 |
| esv2881906 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000010.10 | Chr10 | 104,288,743 | 104,288,777 |
Variant Call Information
| Variant Call ID | Type | Sample ID | Method | Analysis | Other Calls in this Sample and Study |
|---|---|---|---|---|---|
| essv7151473 | insertion | HuRef | Sequencing | Split read mapping | 471,817 |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| essv7151473 | Remapped | Perfect | NC_000010.11:g.102 528986_102529020in sATAAAATTGATTAAATA TAACTGGAGATTTATGGG T | GRCh38.p12 | First Pass | NC_000010.11 | Chr10 | 102,528,986 | 102,529,020 |
| essv7151473 | Submitted genomic | NC_000010.10:g.104 288743_104288777in sATAAAATTGATTAAATA TAACTGGAGATTTATGGG T | GRCh37 (hg19) | NC_000010.10 | Chr10 | 104,288,743 | 104,288,777 |