esv1815595
- 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:323,229
- 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: 742 SVs from 67 studies. See in: genome view
Overlapping variant regions from other studies: 742 SVs from 67 studies. See in: genome view
Overlapping variant regions from other studies: 206 SVs from 19 studies. See in: genome view
Variant Region Placement Information
Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
---|---|---|---|---|---|---|---|---|---|
esv1815595 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000012.12 | Chr12 | 114,959,935 | 115,283,163 |
esv1815595 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000012.11 | Chr12 | 115,397,740 | 115,720,968 |
esv1815595 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000012.10 | Chr12 | 113,882,123 | 114,205,351 |
Variant Call Information
Variant Call Placement Information
Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
---|---|---|---|---|---|---|---|---|---|
essv4374626 | Remapped | Perfect | NC_000012.12:g.(?_ 114959935)_(115283 163_?)del | GRCh38.p12 | First Pass | NC_000012.12 | Chr12 | 114,959,935 | 115,283,163 |
essv4374626 | Remapped | Perfect | NC_000012.11:g.(?_ 115397740)_(115720 968_?)del | GRCh37.p13 | First Pass | NC_000012.11 | Chr12 | 115,397,740 | 115,720,968 |
essv4374626 | Submitted genomic | NC_000012.10:g.(?_ 113882123)_(114205 351_?)del | NCBI36 (hg18) | NC_000012.10 | Chr12 | 113,882,123 | 114,205,351 |