esv1005820
- Organism: Homo sapiens
- Study:estd180 (Pang et al. 2010)
- Variant Type:copy number variation
- Method Type:Oligo aCGH
- Submitted on:NCBI36 (hg18)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:115,945
- Publication(s):Pang et al. 2010
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: 1217 SVs from 74 studies. See in: genome view
Overlapping variant regions from other studies: 1282 SVs from 79 studies. See in: genome view
Overlapping variant regions from other studies: 766 SVs from 27 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 |
---|---|---|---|---|---|---|---|---|---|
esv1005820 | Remapped | Pass | GRCh38.p12 | Primary Assembly | First Pass | NC_000009.12 | Chr9 | 42,224,096 | 42,340,040 |
esv1005820 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000009.11 | Chr9 | 43,386,292 | 43,590,293 |
esv1005820 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000009.10 | Chr9 | 43,326,288 | 43,530,289 |
Variant Call Information
Variant Call Placement Information
Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
---|---|---|---|---|---|---|---|---|---|
essv3587158 | Remapped | Pass | NC_000009.12:g.(?_ 42224096)_(4234004 0_?)del | GRCh38.p12 | First Pass | NC_000009.12 | Chr9 | 42,224,096 | 42,340,040 |
essv3587158 | Remapped | Perfect | NC_000009.11:g.(?_ 43386292)_(4359029 3_?)del | GRCh37.p13 | First Pass | NC_000009.11 | Chr9 | 43,386,292 | 43,590,293 |
essv3587158 | Submitted genomic | NC_000009.10:g.(?_ 43326288)_(4353028 9_?)del | NCBI36 (hg18) | NC_000009.10 | Chr9 | 43,326,288 | 43,530,289 |