esv29979
- 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:1,072,288
- 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: 2362 SVs from 97 studies. See in: genome view
Overlapping variant regions from other studies: 2362 SVs from 97 studies. See in: genome view
Overlapping variant regions from other studies: 680 SVs from 30 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 |
---|---|---|---|---|---|---|---|---|---|
esv29979 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000002.12 | Chr2 | 19,408,886 | 20,481,173 |
esv29979 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000002.11 | Chr2 | 19,608,647 | 20,680,934 |
esv29979 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000002.10 | Chr2 | 19,472,128 | 20,544,415 |
Variant Call Information
Variant Call Placement Information
Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
---|---|---|---|---|---|---|---|---|---|
essv84218 | Remapped | Perfect | NC_000002.12:g.(?_ 19408886)_(2048117 3_?)del | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 19,408,886 | 20,481,173 |
essv84218 | Remapped | Perfect | NC_000002.11:g.(?_ 19608647)_(2068093 4_?)del | GRCh37.p13 | First Pass | NC_000002.11 | Chr2 | 19,608,647 | 20,680,934 |
essv84218 | Submitted genomic | NC_000002.10:g.(?_ 19472128)_(2054441 5_?)del | NCBI36 (hg18) | NC_000002.10 | Chr2 | 19,472,128 | 20,544,415 |