nsv7143826
- Organism: Homo sapiens
- Study:nstd232 (Keane et al. 2023)
- Variant Type:copy number variation
- Method Type:Sequencing
- Submitted on:GRCh37
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:132
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: 352 SVs from 49 studies. See in: genome view
Overlapping variant regions from other studies: 352 SVs from 49 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nsv7143826 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000004.12 | Chr4 | 1,372,729 | 1,372,860 |
| nsv7143826 | Submitted genomic | GRCh37.p13 | Primary Assembly | NC_000004.11 | Chr4 | 1,366,517 | 1,366,648 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis |
|---|---|---|---|
| nssv18837615 | deletion | Sequencing | Sequence alignment |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv18837615 | Remapped | Perfect | NC_000004.12:g.137 2729_1372860del | GRCh38.p12 | First Pass | NC_000004.12 | Chr4 | 1,372,729 | 1,372,860 |
| nssv18837615 | Submitted genomic | NC_000004.11:g.136 6517_1366648del | GRCh37.p13 | NC_000004.11 | Chr4 | 1,366,517 | 1,366,648 |
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) |
|---|---|---|---|
| nssv18837615 | 1 | 3 | 4 |