nsv5902132
- 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:11,649
- 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: 369 SVs from 68 studies. See in: genome view
Overlapping variant regions from other studies: 369 SVs from 68 studies. See in: genome view
Variant Region Placement Information
Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
---|---|---|---|---|---|---|---|---|---|
nsv5902132 | Submitted genomic | GRCh38 (hg38) | Primary Assembly | NC_000003.12 | Chr3 | 114,938,105 | 114,949,753 | ||
nsv5902132 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000003.11 | Chr3 | 114,656,952 | 114,668,600 |
Variant Call Information
Variant Call ID | Type | Method | Analysis |
---|---|---|---|
nssv17396887 | deletion | Sequencing | Sequence alignment |
Variant Call Placement Information
Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
---|---|---|---|---|---|---|---|---|---|
nssv17396887 | Submitted genomic | NC_000003.12:g.114 938105_114949753de l | GRCh38 (hg38) | NC_000003.12 | Chr3 | 114,938,105 | 114,949,753 | ||
nssv17396887 | Remapped | Perfect | NC_000003.11:g.114 656952_114668600de l | GRCh37.p13 | First Pass | NC_000003.11 | Chr3 | 114,656,952 | 114,668,600 |