esv3361836
- Organism: Homo sapiens
- Study:estd59 (1000 Genomes Consortium Pilot Project)
- Variant Type:insertion
- Method Type:Sequencing
- Submitted on:NCBI36 (hg18)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:115
- Publication(s):1000 Genomes Project Consortium et al. 2010
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: 51 SVs from 24 studies. See in: genome view
Overlapping variant regions from other studies: 51 SVs from 24 studies. See in: genome view
Overlapping variant regions from other studies: 12 SVs from 6 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| esv3361836 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000011.10 | Chr11 | 16,064,365 (-90, +90) | 16,064,479 (-92, +90) |
| esv3361836 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000011.9 | Chr11 | 16,085,911 (-90, +90) | 16,086,025 (-92, +90) |
| esv3361836 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000011.8 | Chr11 | 16,042,487 (-90, +90) | 16,042,601 (-92, +90) |
Variant Call Information
| Variant Call ID | Type | Sample ID | Method | Analysis | Other Calls in this Sample and Study |
|---|---|---|---|---|---|
| essv8672012 | insertion | SAMN00001694 | Sequencing | Paired-end mapping | 29,487 |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| essv8672012 | Remapped | Perfect | NC_000011.10:g.(16 064275_16064455)_( 16064387_16064569) ins284 | GRCh38.p12 | First Pass | NC_000011.10 | Chr11 | 16,064,365 (-90, +90) | 16,064,479 (-92, +90) |
| essv8672012 | Remapped | Perfect | NC_000011.9:g.(160 85821_16086001)_(1 6085933_16086115)i ns284 | GRCh37.p13 | First Pass | NC_000011.9 | Chr11 | 16,085,911 (-90, +90) | 16,086,025 (-92, +90) |
| essv8672012 | Submitted genomic | NC_000011.8:g.(160 42397_16042577)_(1 6042509_16042691)i ns284 | NCBI36 (hg18) | NC_000011.8 | Chr11 | 16,042,487 (-90, +90) | 16,042,601 (-92, +90) |