nsv5894158
- 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:4,788
- 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: 356 SVs from 71 studies. See in: genome view
Overlapping variant regions from other studies: 356 SVs from 71 studies. See in: genome view
Variant Region Placement Information
Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
---|---|---|---|---|---|---|---|---|---|
nsv5894158 | Submitted genomic | GRCh38 (hg38) | Primary Assembly | NC_000004.12 | Chr4 | 118,204,256 | 118,209,043 | ||
nsv5894158 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000004.11 | Chr4 | 119,125,411 | 119,130,198 |
Variant Call Information
Variant Call ID | Type | Method | Analysis |
---|---|---|---|
nssv17410668 | deletion | Sequencing | Sequence alignment |
Variant Call Placement Information
Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
---|---|---|---|---|---|---|---|---|---|
nssv17410668 | Submitted genomic | NC_000004.12:g.118 204256_118209043de l | GRCh38 (hg38) | NC_000004.12 | Chr4 | 118,204,256 | 118,209,043 | ||
nssv17410668 | Remapped | Perfect | NC_000004.11:g.119 125411_119130198de l | GRCh37.p13 | First Pass | NC_000004.11 | Chr4 | 119,125,411 | 119,130,198 |