esv3792272
- Organism: Homo sapiens
- Study:estd192 (COSMIC)
- Variant Type:insertion
- Method Type:Curated
- Submitted on:GRCh37
- Variant Calls:2
- Validation:Not tested
- Clinical Assertions: No
- Region Size:245,485
- Description:Chr16:g.47523141_47768625ins
- Publication(s):Forbes et al. 2008, Forbes et al. 2008
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: 414 SVs from 56 studies. See in: genome view
Overlapping variant regions from other studies: 414 SVs from 56 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| esv3792272 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000016.10 | Chr16 | 47,489,230 | 47,734,714 |
| esv3792272 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000016.9 | Chr16 | 47,523,141 | 47,768,625 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| essv16619449 | Remapped | Perfect | NC_000016.10:g.474 89230_47734714ins? | GRCh38.p12 | First Pass | NC_000016.10 | Chr16 | 47,489,230 | 47,734,714 |
| essv16619450 | Remapped | Perfect | NC_000016.10:g.474 89230_47734714ins? | GRCh38.p12 | First Pass | NC_000016.10 | Chr16 | 47,489,230 | 47,734,714 |
| essv16619449 | Submitted genomic | NC_000016.9:g.4752 3141_47768625ins? | GRCh37 (hg19) | NC_000016.9 | Chr16 | 47,523,141 | 47,768,625 | ||
| essv16619450 | Submitted genomic | NC_000016.9:g.4752 3141_47768625ins? | GRCh37 (hg19) | NC_000016.9 | Chr16 | 47,523,141 | 47,768,625 |