nsv5037298
- Organism: Homo sapiens
- Study:nstd200 (Abel et al. 2020)
- Variant Type:inversion
- Method Type:Sequencing
- Submitted on:GRCh38
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:24,034
- Publication(s):Abel et al. 2020
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: 178 SVs from 42 studies. See in: genome view
Overlapping variant regions from other studies: 178 SVs from 42 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nsv5037298 | Submitted genomic | GRCh38 (hg38) | Primary Assembly | NC_000007.14 | Chr7 | 134,635,433 (-5) | 134,659,466 (-3) | ||
| nsv5037298 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000007.13 | Chr7 | 134,320,185 (-5) | 134,344,218 (-3) |
Variant Call Information
| Variant Call ID | Type | Method | Analysis |
|---|---|---|---|
| nssv16516340 | inversion | Sequencing | Sequence alignment |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv16516340 | Submitted genomic | NC_000007.14:g.(13 4635428_?)_(134659 463_?)inv | GRCh38 (hg38) | NC_000007.14 | Chr7 | 134,635,433 (-5) | 134,659,466 (-3) | ||
| nssv16516340 | Remapped | Perfect | NC_000007.13:g.(13 4320180_?)_(134344 215_?)inv | GRCh37.p13 | First Pass | NC_000007.13 | Chr7 | 134,320,185 (-5) | 134,344,218 (-3) |
No validation data were submitted for this variant
No clinical assertion data were submitted for this variant
Genotype Information
| Variant Call ID | Allele Frequency (AF) | Allele Count (AC) | Allele Number (AN) |
|---|---|---|---|
| nssv16516340 | <0.001 | 1 | 29246 |