esv29984
- 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:113,003
- 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: 1123 SVs from 79 studies. See in: genome view
Overlapping variant regions from other studies: 1123 SVs from 79 studies. See in: genome view
Overlapping variant regions from other studies: 392 SVs from 21 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 |
|---|---|---|---|---|---|---|---|---|---|
| esv29984 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000004.12 | Chr4 | 857,569 | 970,571 |
| esv29984 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000004.11 | Chr4 | 851,357 | 964,359 |
| esv29984 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000004.10 | Chr4 | 841,357 | 954,359 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| essv84223 | Remapped | Perfect | NC_000004.12:g.(?_ 857569)_(970571_?) del | GRCh38.p12 | First Pass | NC_000004.12 | Chr4 | 857,569 | 970,571 |
| essv84223 | Remapped | Perfect | NC_000004.11:g.(?_ 851357)_(964359_?) del | GRCh37.p13 | First Pass | NC_000004.11 | Chr4 | 851,357 | 964,359 |
| essv84223 | Submitted genomic | NC_000004.10:g.(?_ 841357)_(954359_?) del | NCBI36 (hg18) | NC_000004.10 | Chr4 | 841,357 | 954,359 |