nsv5328888
- 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:121,174
- 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: 438 SVs from 54 studies. See in: genome view
Overlapping variant regions from other studies: 438 SVs from 54 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nsv5328888 | Submitted genomic | GRCh38.p13 | Primary Assembly | NC_000005.10 | Chr5 | 124,425,508 (-3, +5) | 124,546,681 (-10, +9) | ||
| nsv5328888 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000005.9 | Chr5 | 123,761,201 (-3, +5) | 123,882,374 (-10, +9) |
Variant Call Information
| Variant Call ID | Type | Method | Analysis |
|---|---|---|---|
| nssv16746566 | 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 |
|---|---|---|---|---|---|---|---|---|---|
| nssv16746566 | Submitted genomic | NC_000005.10:g.(12 4425505_124425513) _(124546671_124546 690)inv | GRCh38.p13 | NC_000005.10 | Chr5 | 124,425,508 (-3, +5) | 124,546,681 (-10, +9) | ||
| nssv16746566 | Remapped | Perfect | NC_000005.9:g.(123 761198_123761206)_ (123882364_1238823 83)inv | GRCh37.p13 | First Pass | NC_000005.9 | Chr5 | 123,761,201 (-3, +5) | 123,882,374 (-10, +9) |
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) |
|---|---|
| nssv16746566 | <0.001 |