esv3768428
- Organism: Homo sapiens
- Study:estd192 (COSMIC)
- Variant Type:copy number variation
- Method Type:Curated
- Submitted on:GRCh37
- Variant Calls:2
- Validation:Not tested
- Clinical Assertions: No
- Region Size:399,054
- Description:
Chr6:g.(124477413_124477433)_(124876447_124876467)del - 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: 1068 SVs from 82 studies. See in: genome view
Overlapping variant regions from other studies: 1069 SVs from 82 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Outer Start | Inner Start | Inner Stop | Outer Stop |
|---|---|---|---|---|---|---|---|---|---|---|---|
| esv3768428 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000006.12 | Chr6 | 124,156,268 | 124,156,268 | 124,555,321 | 124,555,321 |
| esv3768428 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000006.11 | Chr6 | 124,477,413 | 124,477,433 | 124,876,447 | 124,876,467 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Outer Start | Inner Start | Inner Stop | Outer Stop |
|---|---|---|---|---|---|---|---|---|---|---|---|
| essv16592943 | Remapped | Perfect | NC_000006.12:g.(12 4156268_124156268) _(124555321_124555 321)del | GRCh38.p12 | First Pass | NC_000006.12 | Chr6 | 124,156,268 | 124,156,268 | 124,555,321 | 124,555,321 |
| essv16592944 | Remapped | Perfect | NC_000006.12:g.(12 4156268_124156268) _(124555321_124555 321)del | GRCh38.p12 | First Pass | NC_000006.12 | Chr6 | 124,156,268 | 124,156,268 | 124,555,321 | 124,555,321 |
| essv16592943 | Submitted genomic | NC_000006.11:g.(12 4477413_124477433) _(124876447_124876 467)del | GRCh37 (hg19) | NC_000006.11 | Chr6 | 124,477,413 | 124,477,433 | 124,876,447 | 124,876,467 | ||
| essv16592944 | Submitted genomic | NC_000006.11:g.(12 4477413_124477433) _(124876447_124876 467)del | GRCh37 (hg19) | NC_000006.11 | Chr6 | 124,477,413 | 124,477,433 | 124,876,447 | 124,876,467 |