esv3674297
- Organism: Homo sapiens
- Study:estd217 (Besenbacher et al. 2015)
- Variant Type:sequence alteration
- Method Type:Sequencing
- Submitted on:GRCh37 (hg19)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:1,871
- Publication(s):Besenbacher et al. 2015
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: 369 SVs from 26 studies. See in: genome view
Overlapping variant regions from other studies: 369 SVs from 26 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| esv3674297 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000023.11 | ChrX | 71,349,454 | 71,351,324 |
| esv3674297 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000023.10 | ChrX | 70,569,304 | 70,571,174 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis |
|---|---|---|---|
| essv16496071 | sequence alteration | Sequencing | de novo sequence assembly |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|
| essv16496071 | Remapped | Perfect | GRCh38.p12 | First Pass | NC_000023.11 | ChrX | 71,349,454 | 71,351,324 |
| essv16496071 | Submitted genomic | GRCh37 (hg19) | NC_000023.10 | ChrX | 70,569,304 | 70,571,174 |