esv3888677
- Organism: Homo sapiens
- Study:estd219 (1000 Genomes Consortium Phase 3 Integrated SV)
- Variant Type: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: 419 SVs from 24 studies. See in: genome view
Overlapping variant regions from other studies: 420 SVs from 24 studies. See in: genome view
Variant Region Placement Information
Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
---|---|---|---|---|---|---|---|---|---|
esv3888677 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000023.11 | ChrX | 36,274,806 (-0, +270) | 36,274,806 (-270, +0) |
esv3888677 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000023.10 | ChrX | 36,292,921 (-0, +270) | 36,292,921 (-270, +0) |
Variant Call Information
Variant Call Placement Information
Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
---|---|---|---|---|---|---|---|---|---|
essv25282544 | Remapped | Perfect | NC_000023.11:g.(36 274806_36275076)_( 36274536_36274806) ins5358 | GRCh38.p12 | First Pass | NC_000023.11 | ChrX | 36,274,806 (-0, +270) | 36,274,806 (-270, +0) |
essv25282544 | Submitted genomic | NC_000023.10:g.(36 292921_36293191)_( 36292651_36292921) ins5358 | GRCh37 (hg19) | NC_000023.10 | ChrX | 36,292,921 (-0, +270) | 36,292,921 (-270, +0) |