esv3870304
- 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: 219 SVs from 27 studies. See in: genome view
Overlapping variant regions from other studies: 219 SVs from 27 studies. See in: genome view
Variant Region Placement Information
Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
---|---|---|---|---|---|---|---|---|---|
esv3870304 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000013.11 | Chr13 | 49,238,696 (-0, +3) | 49,238,696 (-3, +0) |
esv3870304 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000013.10 | Chr13 | 49,812,832 (-0, +3) | 49,812,832 (-3, +0) |
Variant Call Information
Variant Call Placement Information
Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
---|---|---|---|---|---|---|---|---|---|
essv23126575 | Remapped | Perfect | NC_000013.11:g.(49 238696_49238699)_( 49238693_49238696) ins1466 | GRCh38.p12 | First Pass | NC_000013.11 | Chr13 | 49,238,696 (-0, +3) | 49,238,696 (-3, +0) |
essv23126575 | Submitted genomic | NC_000013.10:g.(49 812832_49812835)_( 49812829_49812832) ins1466 | GRCh37 (hg19) | NC_000013.10 | Chr13 | 49,812,832 (-0, +3) | 49,812,832 (-3, +0) |