nsv5925476
- 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:2,171,568
- 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: 4778 SVs from 108 studies. See in: genome view
Overlapping variant regions from other studies: 15602 SVs from 133 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nsv5925476 | Submitted genomic | GRCh38 (hg38) | Primary Assembly | NC_000007.14 | Chr7 | 60,340,898 | 62,512,465 | ||
| nsv5925476 | Remapped | Pass | GRCh37.p13 | Primary Assembly | Second Pass | NC_000007.13 | Chr7 | 61,646,111 | 64,968,413 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis |
|---|---|---|---|
| nssv17433838 | deletion | Sequencing | Sequence alignment |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv17433838 | Submitted genomic | NC_000007.14:g.603 40898_62512465del | GRCh38 (hg38) | NC_000007.14 | Chr7 | 60,340,898 | 62,512,465 | ||
| nssv17433838 | Remapped | Pass | NC_000007.13:g.616 46111_64968413del | GRCh37.p13 | Second Pass | NC_000007.13 | Chr7 | 61,646,111 | 64,968,413 |