esv23382
- Organism: Homo sapiens
- Study:estd20 (Conrad et al. 2009)
- Variant Type:sequence alteration
- Method Type:Oligo aCGH
- Submitted on:NCBI36 (hg18)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:838
- Publication(s):Conrad et al. 2009
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: 170 SVs from 20 studies. See in: genome view
Overlapping variant regions from other studies: 170 SVs from 20 studies. See in: genome view
Overlapping variant regions from other studies: 73 SVs from 10 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 |
---|---|---|---|---|---|---|---|---|---|
esv23382 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000019.10 | Chr19 | 33,621,577 | 33,622,414 |
esv23382 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000019.9 | Chr19 | 34,112,483 | 34,113,320 |
esv23382 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000019.8 | Chr19 | 38,804,323 | 38,805,160 |
Variant Call Information
Variant Call ID | Type | Method |
---|---|---|
esv11860 | copy number variation | Merged region |
Variant Call Placement Information
Variant Call ID | Placement Type | Score | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
---|---|---|---|---|---|---|---|---|
esv11860 | Remapped | Perfect | GRCh38.p12 | First Pass | NC_000019.10 | Chr19 | 33,621,577 | 33,622,414 |
esv11860 | Remapped | Perfect | GRCh37.p13 | First Pass | NC_000019.9 | Chr19 | 34,112,483 | 34,113,320 |
esv11860 | Submitted genomic | NCBI36 (hg18) | NC_000019.8 | Chr19 | 38,804,323 | 38,805,160 |