esv3889801
- 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: 421 SVs from 27 studies. See in: genome view
Overlapping variant regions from other studies: 420 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 | Start | Stop |
---|---|---|---|---|---|---|---|---|---|
esv3889801 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000023.11 | ChrX | 113,107,844 | 113,107,844 |
esv3889801 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000023.10 | ChrX | 112,351,072 | 112,351,072 |
Variant Call Information
Variant Call Placement Information
Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
---|---|---|---|---|---|---|---|---|---|
essv25547898 | Remapped | Perfect | NC_000023.11:g.113 107844_113107845in s5909 | GRCh38.p12 | First Pass | NC_000023.11 | ChrX | 113,107,844 | 113,107,844 |
essv25547898 | Submitted genomic | NC_000023.10:g.112 351072_112351073in s5909 | GRCh37 (hg19) | NC_000023.10 | ChrX | 112,351,072 | 112,351,072 |