esv3825805
- 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:221,965
- 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: 677 SVs from 65 studies. See in: genome view
Overlapping variant regions from other studies: 678 SVs from 65 studies. See in: genome view
Variant Region Placement Information
Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
---|---|---|---|---|---|---|---|---|---|
esv3825805 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000002.12 | Chr2 | 120,815,398 | 121,037,362 |
esv3825805 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000002.11 | Chr2 | 121,572,973 | 121,794,938 |
Variant Call Information
Variant Call Placement Information
Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
---|---|---|---|---|---|---|---|---|---|
essv17820853 | Remapped | Perfect | NC_000002.12:g.120 815398_121037362du p | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 120,815,398 | 121,037,362 |
essv17820853 | Submitted genomic | NC_000002.11:g.121 572973_121794938du p | GRCh37 (hg19) | NC_000002.11 | Chr2 | 121,572,973 | 121,794,938 |