esv3832853
- Organism: Homo sapiens
- Study:estd219 (1000 Genomes Consortium Phase 3 Integrated SV)
- Variant Type:copy number variation
- Method Type:Sequencing
- Submitted on:GRCh37
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:251,683
- 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: 813 SVs from 67 studies. See in: genome view
Overlapping variant regions from other studies: 813 SVs from 67 studies. See in: genome view
Variant Region Placement Information
Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
---|---|---|---|---|---|---|---|---|---|
esv3832853 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000003.12 | Chr3 | 163,440,740 | 163,692,422 |
esv3832853 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000003.11 | Chr3 | 163,158,528 | 163,410,210 |
Variant Call Information
Variant Call Placement Information
Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
---|---|---|---|---|---|---|---|---|---|
essv18580484 | Remapped | Perfect | NC_000003.12:g.163 440740_163692422de l | GRCh38.p12 | First Pass | NC_000003.12 | Chr3 | 163,440,740 | 163,692,422 |
essv18580484 | Submitted genomic | NC_000003.11:g.163 158528_163410210de l | GRCh37 (hg19) | NC_000003.11 | Chr3 | 163,158,528 | 163,410,210 |