esv3889755
- Organism: Homo sapiens
- Study:estd219 (1000 Genomes Consortium Phase 3 Integrated SV)
- Variant Type:mobile element insertion
- Method Type:Sequencing
- Submitted on:GRCh37
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:1
- Publication(s):1000 Genomes Consortium Phase 3 Integrated SV
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: 428 SVs from 30 studies. See in: genome view
Overlapping variant regions from other studies: 428 SVs from 30 studies. See in: genome view
Variant Region Placement Information
Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
---|---|---|---|---|---|---|---|---|---|
esv3889755 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000023.11 | ChrX | 109,727,339 | 109,727,339 |
esv3889755 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000023.10 | ChrX | 108,970,568 | 108,970,568 |
Variant Call Information
Variant Call Placement Information
Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
---|---|---|---|---|---|---|---|---|---|
essv25535931 | Remapped | Perfect | NC_000023.11:g.109 727339_109727340in s1541 | GRCh38.p12 | First Pass | NC_000023.11 | ChrX | 109,727,339 | 109,727,339 |
essv25535931 | Submitted genomic | NC_000023.10:g.108 970568_108970569in s1541 | GRCh37 (hg19) | NC_000023.10 | ChrX | 108,970,568 | 108,970,568 |