nsv5325627
- Organism: Homo sapiens
- Study:nstd204 (Chen et al. 2021)
- Variant Type:inversion
- Method Type:Sequencing
- Submitted on:GRCh38
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:2,652,082
- Publication(s):Chen et al. 2021
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: 6727 SVs from 117 studies. See in: genome view
Overlapping variant regions from other studies: 6727 SVs from 117 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nsv5325627 | Submitted genomic | GRCh38.p13 | Primary Assembly | NC_000011.10 | Chr11 | 58,901,988 (-8, +9) | 61,554,069 (-2) | ||
| nsv5325627 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000011.9 | Chr11 | 58,669,461 (-8, +9) | 61,321,541 (-2) |
Variant Call Information
| Variant Call ID | Type | Method | Analysis |
|---|---|---|---|
| nssv16742041 | inversion | Sequencing | Split read and paired-end mapping |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv16742041 | Submitted genomic | NC_000011.10:g.(58 901980_58901997)_( 61554067_?)inv | GRCh38.p13 | NC_000011.10 | Chr11 | 58,901,988 (-8, +9) | 61,554,069 (-2) | ||
| nssv16742041 | Remapped | Perfect | NC_000011.9:g.(586 69453_58669470)_(6 1321539_?)inv | GRCh37.p13 | First Pass | NC_000011.9 | Chr11 | 58,669,461 (-8, +9) | 61,321,541 (-2) |
No validation data were submitted for this variant
No clinical assertion data were submitted for this variant
Complete genotype and/or allele frequency data for this study can be found on dbVar's FTP site.
Genotype Information
| Variant Call ID | Allele Frequency (AF) |
|---|---|
| nssv16742041 | <0.001 |