esv29988
- 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:42,836
- 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: 1149 SVs from 89 studies. See in: genome view
Overlapping variant regions from other studies: 1149 SVs from 89 studies. See in: genome view
Overlapping variant regions from other studies: 720 SVs from 29 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 |
---|---|---|---|---|---|---|---|---|---|
esv29988 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000001.11 | Chr1 | 16,882,837 | 16,925,672 |
esv29988 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000001.10 | Chr1 | 17,209,332 | 17,252,167 |
esv29988 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000001.9 | Chr1 | 17,081,919 | 17,124,754 |
Variant Call Information
Variant Call Placement Information
Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
---|---|---|---|---|---|---|---|---|---|
essv84227 | Remapped | Perfect | NC_000001.11:g.(?_ 16882837)_(1692567 2_?)del | GRCh38.p12 | First Pass | NC_000001.11 | Chr1 | 16,882,837 | 16,925,672 |
essv84227 | Remapped | Perfect | NC_000001.10:g.(?_ 17209332)_(1725216 7_?)del | GRCh37.p13 | First Pass | NC_000001.10 | Chr1 | 17,209,332 | 17,252,167 |
essv84227 | Submitted genomic | NC_000001.9:g.(?_1 7081919)_(17124754 _?)del | NCBI36 (hg18) | NC_000001.9 | Chr1 | 17,081,919 | 17,124,754 |