esv29966
- 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:197,353
- 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: 640 SVs from 74 studies. See in: genome view
Overlapping variant regions from other studies: 640 SVs from 74 studies. See in: genome view
Overlapping variant regions from other studies: 211 SVs from 18 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 |
|---|---|---|---|---|---|---|---|---|---|
| esv29966 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000001.11 | Chr1 | 10,616,743 | 10,814,095 |
| esv29966 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000001.10 | Chr1 | 10,676,800 | 10,874,152 |
| esv29966 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000001.9 | Chr1 | 10,599,387 | 10,796,739 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| essv84205 | Remapped | Perfect | NC_000001.11:g.(?_ 10616743)_(1081409 5_?)del | GRCh38.p12 | First Pass | NC_000001.11 | Chr1 | 10,616,743 | 10,814,095 |
| essv84205 | Remapped | Perfect | NC_000001.10:g.(?_ 10676800)_(1087415 2_?)del | GRCh37.p13 | First Pass | NC_000001.10 | Chr1 | 10,676,800 | 10,874,152 |
| essv84205 | Submitted genomic | NC_000001.9:g.(?_1 0599387)_(10796739 _?)del | NCBI36 (hg18) | NC_000001.9 | Chr1 | 10,599,387 | 10,796,739 |