nsv7138903
- 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:114
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: 264 SVs from 37 studies. See in: genome view
Overlapping variant regions from other studies: 264 SVs from 37 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nsv7138903 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000009.12 | Chr9 | 137,819,487 | 137,819,600 |
| nsv7138903 | Submitted genomic | GRCh37.p13 | Primary Assembly | NC_000009.11 | Chr9 | 140,713,939 | 140,714,052 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis |
|---|---|---|---|
| nssv18833766 | deletion | Sequencing | Sequence alignment |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv18833766 | Remapped | Perfect | NC_000009.12:g.137 819487_137819600de l | GRCh38.p12 | First Pass | NC_000009.12 | Chr9 | 137,819,487 | 137,819,600 |
| nssv18833766 | Submitted genomic | NC_000009.11:g.140 713939_140714052de l | GRCh37.p13 | NC_000009.11 | Chr9 | 140,713,939 | 140,714,052 |
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) |
|---|---|---|---|
| nssv18833766 | 0.5 | 1 | 2 |