esv1826827
- Organism: Homo sapiens
- Study:estd188 (Pinto et al. 2011)
- Variant Type:copy number variation
- Method Type:Oligo aCGH
- Submitted on:NCBI36 (hg18)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:190,084
- Publication(s):Pinto et al. 2011
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: 931 SVs from 91 studies. See in: genome view
Overlapping variant regions from other studies: 931 SVs from 91 studies. See in: genome view
Overlapping variant regions from other studies: 291 SVs from 29 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 |
|---|---|---|---|---|---|---|---|---|---|---|
| esv1826827 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000004.12 | Chr4 | 167,875,974 | 167,889,044 | 168,066,057 |
| esv1826827 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000004.11 | Chr4 | 168,797,125 | 168,810,195 | 168,987,208 |
| esv1826827 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000004.10 | Chr4 | 169,033,700 | 169,046,770 | 169,223,783 |
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 |
|---|---|---|---|---|---|---|---|---|---|---|
| essv4424275 | Remapped | Perfect | NC_000004.12:g.(16 7875974_167889044) _(168066057_?)dup | GRCh38.p12 | First Pass | NC_000004.12 | Chr4 | 167,875,974 | 167,889,044 | 168,066,057 |
| essv4424275 | Remapped | Perfect | NC_000004.11:g.(16 8797125_168810195) _(168987208_?)dup | GRCh37.p13 | First Pass | NC_000004.11 | Chr4 | 168,797,125 | 168,810,195 | 168,987,208 |
| essv4424275 | Submitted genomic | NC_000004.10:g.(16 9033700_169046770) _(169223783_?)dup | NCBI36 (hg18) | NC_000004.10 | Chr4 | 169,033,700 | 169,046,770 | 169,223,783 |