esv29989
- 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:12,073
- 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: 444 SVs from 77 studies. See in: genome view
Overlapping variant regions from other studies: 443 SVs from 77 studies. See in: genome view
Overlapping variant regions from other studies: 213 SVs from 24 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 |
|---|---|---|---|---|---|---|---|---|---|
| esv29989 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000003.12 | Chr3 | 52,992,698 | 53,004,770 |
| esv29989 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000003.11 | Chr3 | 53,026,714 | 53,038,786 |
| esv29989 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000003.10 | Chr3 | 53,001,754 | 53,013,826 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| essv84228 | Remapped | Perfect | NC_000003.12:g.(?_ 52992698)_(5300477 0_?)del | GRCh38.p12 | First Pass | NC_000003.12 | Chr3 | 52,992,698 | 53,004,770 |
| essv84228 | Remapped | Perfect | NC_000003.11:g.(?_ 53026714)_(5303878 6_?)del | GRCh37.p13 | First Pass | NC_000003.11 | Chr3 | 53,026,714 | 53,038,786 |
| essv84228 | Submitted genomic | NC_000003.10:g.(?_ 53001754)_(5301382 6_?)del | NCBI36 (hg18) | NC_000003.10 | Chr3 | 53,001,754 | 53,013,826 |