esv29970
- Organism: Homo sapiens
- Study:estd22 (Levy et al. 2007)
- Variant Type:copy number variation
- Method Type:Oligo aCGH, SNP array
- Submitted on:NCBI36 (hg18)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:28,078
- Publication(s):Levy et al. 2007
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: 743 SVs from 90 studies. See in: genome view
Overlapping variant regions from other studies: 743 SVs from 90 studies. See in: genome view
Overlapping variant regions from other studies: 401 SVs from 32 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 |
|---|---|---|---|---|---|---|---|---|---|
| esv29970 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000016.10 | Chr16 | 70,134,953 | 70,163,030 |
| esv29970 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000016.9 | Chr16 | 70,168,856 | 70,196,933 |
| esv29970 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000016.8 | Chr16 | 68,726,357 | 68,754,434 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| essv84209 | Remapped | Perfect | NC_000016.10:g.(?_ 70134953)_(7016303 0_?)del | GRCh38.p12 | First Pass | NC_000016.10 | Chr16 | 70,134,953 | 70,163,030 |
| essv84209 | Remapped | Perfect | NC_000016.9:g.(?_7 0168856)_(70196933 _?)del | GRCh37.p13 | First Pass | NC_000016.9 | Chr16 | 70,168,856 | 70,196,933 |
| essv84209 | Submitted genomic | NC_000016.8:g.(?_6 8726357)_(68754434 _?)del | NCBI36 (hg18) | NC_000016.8 | Chr16 | 68,726,357 | 68,754,434 |