esv3810376
- Organism: Homo sapiens
- Study:estd192 (COSMIC)
- Variant Type:inversion
- Method Type:Curated
- Submitted on:GRCh37
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:110,442
- Description:Chr9:g.16607940_16718381inv
- Publication(s):Berger et al. 2011, 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: 532 SVs from 57 studies. See in: genome view
Overlapping variant regions from other studies: 536 SVs from 57 studies. See in: genome view
Variant Region Placement Information
Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
---|---|---|---|---|---|---|---|---|---|
esv3810376 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000009.12 | Chr9 | 16,607,942 | 16,718,383 |
esv3810376 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000009.11 | Chr9 | 16,607,940 | 16,718,381 |
Variant Call Information
Variant Call ID | Type | Sample ID | Method | Analysis | Other Calls in this Sample and Study |
---|---|---|---|---|---|
essv16639691 | inversion | 1669609 | Curated | Curated | 80 |
Variant Call Placement Information
Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
---|---|---|---|---|---|---|---|---|---|
essv16639691 | Remapped | Perfect | NC_000009.12:g.166 07942_16718383inv | GRCh38.p12 | First Pass | NC_000009.12 | Chr9 | 16,607,942 | 16,718,383 |
essv16639691 | Submitted genomic | NC_000009.11:g.166 07940_16718381inv | GRCh37 (hg19) | NC_000009.11 | Chr9 | 16,607,940 | 16,718,381 |