esv3812540
- 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:123,890,770
- Description:Chr2:g.99402600_223541625ins
- 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: 289987 SVs from 151 studies. See in: genome view
Overlapping variant regions from other studies: 290193 SVs from 151 studies. See in: genome view
Variant Region Placement Information
Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
---|---|---|---|---|---|---|---|---|---|
esv3812540 | Remapped | Good | GRCh38.p12 | Primary Assembly | First Pass | NC_000002.12 | Chr2 | 98,786,137 | 222,676,906 |
esv3812540 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000002.11 | Chr2 | 99,402,600 | 223,541,625 |
Variant Call Information
Variant Call Placement Information
Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
---|---|---|---|---|---|---|---|---|---|
essv16642113 | Remapped | Good | NC_000002.12:g.987 86137_222676906ins ? | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 98,786,137 | 222,676,906 |
essv16642114 | Remapped | Good | NC_000002.12:g.987 86137_222676906ins ? | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 98,786,137 | 222,676,906 |
essv16642113 | Submitted genomic | NC_000002.11:g.994 02600_223541625ins ? | GRCh37 (hg19) | NC_000002.11 | Chr2 | 99,402,600 | 223,541,625 | ||
essv16642114 | Submitted genomic | NC_000002.11:g.994 02600_223541625ins ? | GRCh37 (hg19) | NC_000002.11 | Chr2 | 99,402,600 | 223,541,625 |