nsv7142833
- Organism: Homo sapiens
- Study:nstd232 (Keane et al. 2023)
- Variant Type:insertion
- Method Type:Sequencing
- Submitted on:GRCh37
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:1
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: 182 SVs from 22 studies. See in: genome view
Overlapping variant regions from other studies: 182 SVs from 22 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nsv7142833 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000008.11 | Chr8 | 22,585,635 | 22,585,635 |
| nsv7142833 | Submitted genomic | GRCh37.p13 | Primary Assembly | NC_000008.10 | Chr8 | 22,443,148 | 22,443,148 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis |
|---|---|---|---|
| nssv18835561 | insertion | Sequencing | Sequence alignment |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv18835561 | Remapped | Perfect | NC_000008.11:g.225 85635_22585636ins8 4 | GRCh38.p12 | First Pass | NC_000008.11 | Chr8 | 22,585,635 | 22,585,635 |
| nssv18835561 | Submitted genomic | NC_000008.10:g.224 43148_22443149ins8 4 | GRCh37.p13 | NC_000008.10 | Chr8 | 22,443,148 | 22,443,148 |
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) |
|---|---|---|---|
| nssv18835561 | 1 | 2 | 2 |