esv3864859
- 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:19,886
- 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: 229 SVs from 47 studies. See in: genome view
Overlapping variant regions from other studies: 229 SVs from 47 studies. See in: genome view
Variant Region Placement Information
Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
---|---|---|---|---|---|---|---|---|---|
esv3864859 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000011.10 | Chr11 | 87,168,333 (-500, +0) | 87,188,218 (-0, +500) |
esv3864859 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000011.9 | Chr11 | 86,879,375 (-500, +0) | 86,899,260 (-0, +500) |
Variant Call Information
Variant Call Placement Information
Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
---|---|---|---|---|---|---|---|---|---|
essv22503218 | Remapped | Perfect | NC_000011.10:g.(87 167833_87168333)_( 87188218_87188718) del | GRCh38.p12 | First Pass | NC_000011.10 | Chr11 | 87,168,333 (-500, +0) | 87,188,218 (-0, +500) |
essv22503218 | Submitted genomic | NC_000011.9:g.(868 78875_86879375)_(8 6899260_86899760)d el | GRCh37 (hg19) | NC_000011.9 | Chr11 | 86,879,375 (-500, +0) | 86,899,260 (-0, +500) |