esv3798820
- Organism: Homo sapiens
- Study:estd192 (COSMIC)
- Variant Type:insertion
- Method Type:Curated
- Submitted on:GRCh37
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:45,303,219
- Description:Chr16:g.50106177_4819049ins
- Publication(s):Forbes et al. 2008, Forbes et al. 2008, Zhang et al. 2012
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: 108900 SVs from 153 studies. See in: genome view
Overlapping variant regions from other studies: 107920 SVs from 153 studies. See in: genome view
Variant Region Placement Information
Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
---|---|---|---|---|---|---|---|---|---|
esv3798820 | Remapped | Good | GRCh38.p12 | Primary Assembly | First Pass | NC_000016.10 | Chr16 | 4,769,048 | 50,072,266 |
esv3798820 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000016.9 | Chr16 | 4,819,049 | 50,106,177 |
Variant Call Information
Variant Call ID | Type | Sample ID | Method | Analysis | Other Calls in this Sample and Study |
---|---|---|---|---|---|
essv16626781 | insertion | 1745787 | Curated | Curated | 15 |
Variant Call Placement Information
Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
---|---|---|---|---|---|---|---|---|---|
essv16626781 | Remapped | Good | NC_000016.10:g.476 9048_50072266ins? | GRCh38.p12 | First Pass | NC_000016.10 | Chr16 | 4,769,048 | 50,072,266 |
essv16626781 | Submitted genomic | NC_000016.9:g.4819 049_50106177ins? | GRCh37 (hg19) | NC_000016.9 | Chr16 | 4,819,049 | 50,106,177 |