nsv5920709
- Organism: Homo sapiens
- Study:nstd209 (Almarri et al. 2020)
- Variant Type:copy number variation
- Method Type:Sequencing
- Submitted on:GRCh38
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:689,410
- Publication(s):Almarri 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: 3044 SVs from 116 studies. See in: genome view
Overlapping variant regions from other studies: 2404 SVs from 113 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nsv5920709 | Submitted genomic | GRCh38 (hg38) | Primary Assembly | NC_000007.14 | Chr7 | 65,106,549 | 65,795,958 | ||
| nsv5920709 | Remapped | Pass | GRCh37.p13 | Primary Assembly | First Pass | NC_000007.13 | Chr7 | 64,566,927 | 65,012,082 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis |
|---|---|---|---|
| nssv17446486 | deletion | Sequencing | Sequence alignment |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv17446486 | Submitted genomic | NC_000007.14:g.651 06549_65795958del | GRCh38 (hg38) | NC_000007.14 | Chr7 | 65,106,549 | 65,795,958 | ||
| nssv17446486 | Remapped | Pass | NC_000007.13:g.645 66927_65012082del | GRCh37.p13 | First Pass | NC_000007.13 | Chr7 | 64,566,927 | 65,012,082 |