nsv5037423
- 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:227,305
- 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: 803 SVs from 74 studies. See in: genome view
Overlapping variant regions from other studies: 803 SVs from 74 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nsv5037423 | Submitted genomic | GRCh38 (hg38) | Primary Assembly | NC_000014.9 | Chr14 | 94,443,376 (+5) | 94,670,680 | ||
| nsv5037423 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000014.8 | Chr14 | 94,909,713 (+5) | 95,137,017 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis |
|---|---|---|---|
| nssv16556777 | inversion | Sequencing | Sequence alignment |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv16556777 | Submitted genomic | NC_000014.9:g.(?_9 4443381)_94670680i nv | GRCh38 (hg38) | NC_000014.9 | Chr14 | 94,443,376 (+5) | 94,670,680 | ||
| nssv16556777 | Remapped | Perfect | NC_000014.8:g.(?_9 4909718)_95137017i nv | GRCh37.p13 | First Pass | NC_000014.8 | Chr14 | 94,909,713 (+5) | 95,137,017 |
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) |
|---|---|---|---|
| nssv16556777 | <0.001 | 1 | 29246 |