esv3887318
- 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: 132 SVs from 30 studies. See in: genome view
Overlapping variant regions from other studies: 132 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 |
---|---|---|---|---|---|---|---|---|---|
esv3887318 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000022.11 | Chr22 | 30,064,907 | 30,064,907 |
esv3887318 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000022.10 | Chr22 | 30,460,896 | 30,460,896 |
Variant Call Information
Variant Call Placement Information
Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
---|---|---|---|---|---|---|---|---|---|
essv25064240 | Remapped | Perfect | NC_000022.11:g.300 64907_30064908ins1 26 | GRCh38.p12 | First Pass | NC_000022.11 | Chr22 | 30,064,907 | 30,064,907 |
essv25064240 | Submitted genomic | NC_000022.10:g.304 60896_30460897ins1 26 | GRCh37 (hg19) | NC_000022.10 | Chr22 | 30,460,896 | 30,460,896 |