esv3766054
- 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:165,519,094
- Description:Chr1:g.39598646_204621195ins
- 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: 341354 SVs from 157 studies. See in: genome view
Overlapping variant regions from other studies: 339827 SVs from 157 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| esv3766054 | Remapped | Good | GRCh38.p12 | Primary Assembly | First Pass | NC_000001.11 | Chr1 | 39,132,974 | 204,652,067 |
| esv3766054 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000001.10 | Chr1 | 39,598,646 | 204,621,195 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| essv16590286 | Remapped | Good | NC_000001.11:g.391 32974_204652067ins ? | GRCh38.p12 | First Pass | NC_000001.11 | Chr1 | 39,132,974 | 204,652,067 |
| essv16590287 | Remapped | Good | NC_000001.11:g.391 32974_204652067ins ? | GRCh38.p12 | First Pass | NC_000001.11 | Chr1 | 39,132,974 | 204,652,067 |
| essv16590286 | Submitted genomic | NC_000001.10:g.395 98646_204621195ins ? | GRCh37 (hg19) | NC_000001.10 | Chr1 | 39,598,646 | 204,621,195 | ||
| essv16590287 | Submitted genomic | NC_000001.10:g.395 98646_204621195ins ? | GRCh37 (hg19) | NC_000001.10 | Chr1 | 39,598,646 | 204,621,195 |