esv29987
- 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:79,652
- 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: 1977 SVs from 92 studies. See in: genome view
Overlapping variant regions from other studies: 1977 SVs from 92 studies. See in: genome view
Overlapping variant regions from other studies: 858 SVs from 28 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 |
|---|---|---|---|---|---|---|---|---|---|
| esv29987 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000006.12 | Chr6 | 269,735 | 349,386 |
| esv29987 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000006.11 | Chr6 | 269,735 | 349,386 |
| esv29987 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000006.10 | Chr6 | 214,735 | 294,386 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| essv84226 | Remapped | Perfect | NC_000006.12:g.(?_ 269735)_(349386_?) del | GRCh38.p12 | First Pass | NC_000006.12 | Chr6 | 269,735 | 349,386 |
| essv84226 | Remapped | Perfect | NC_000006.11:g.(?_ 269735)_(349386_?) del | GRCh37.p13 | First Pass | NC_000006.11 | Chr6 | 269,735 | 349,386 |
| essv84226 | Submitted genomic | NC_000006.10:g.(?_ 214735)_(294386_?) del | NCBI36 (hg18) | NC_000006.10 | Chr6 | 214,735 | 294,386 |