esv29997
- 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:32,323
- 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: 668 SVs from 86 studies. See in: genome view
Overlapping variant regions from other studies: 668 SVs from 86 studies. See in: genome view
Overlapping variant regions from other studies: 354 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 |
|---|---|---|---|---|---|---|---|---|---|
| esv29997 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000001.11 | Chr1 | 25,289,645 | 25,321,967 |
| esv29997 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000001.10 | Chr1 | 25,616,136 | 25,648,458 |
| esv29997 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000001.9 | Chr1 | 25,488,723 | 25,521,045 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| essv84236 | Remapped | Perfect | NC_000001.11:g.(?_ 25289645)_(2532196 7_?)dup | GRCh38.p12 | First Pass | NC_000001.11 | Chr1 | 25,289,645 | 25,321,967 |
| essv84236 | Remapped | Perfect | NC_000001.10:g.(?_ 25616136)_(2564845 8_?)dup | GRCh37.p13 | First Pass | NC_000001.10 | Chr1 | 25,616,136 | 25,648,458 |
| essv84236 | Submitted genomic | NC_000001.9:g.(?_2 5488723)_(25521045 _?)dup | NCBI36 (hg18) | NC_000001.9 | Chr1 | 25,488,723 | 25,521,045 |