esv3572838
- Organism: Homo sapiens
- Study:estd212 (Uddin et al. 2014)
- Variant Type:copy number variation
- Method Type:SNP array
- Submitted on:GRCh37 (hg19)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:351,786
- Publication(s):Uddin et al. 2014
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: 912 SVs from 69 studies. See in: genome view
Overlapping variant regions from other studies: 912 SVs from 69 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 |
---|---|---|---|---|---|---|---|---|---|
esv3572838 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000008.11 | Chr8 | 75,697,821 | 76,049,606 |
esv3572838 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000008.10 | Chr8 | 76,610,056 | 76,961,841 |
Variant Call Information
Variant Call ID | Type | Method | Analysis | Copy number |
---|---|---|---|---|
essv9789061 | copy number loss | SNP array | Probe signal intensity | 1 |
Variant Call Placement Information
Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
---|---|---|---|---|---|---|---|---|---|
essv9789061 | Remapped | Perfect | NC_000008.11:g.(?_ 75697821)_(7604960 6_?)del | GRCh38.p12 | First Pass | NC_000008.11 | Chr8 | 75,697,821 | 76,049,606 |
essv9789061 | Submitted genomic | NC_000008.10:g.(?_ 76610056)_(7696184 1_?)del | GRCh37 (hg19) | NC_000008.10 | Chr8 | 76,610,056 | 76,961,841 |