nsv5844611
- Organism: Homo sapiens
- Study:nstd209 (Almarri et al. 2020)
- Variant Type:copy number variation
- Method Type:Sequencing
- Submitted on:GRCh38
- Variant Calls:3
- Validation:Not tested
- Clinical Assertions: No
- Region Size:3,562
- 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: 435 SVs from 55 studies. See in: genome view
Overlapping variant regions from other studies: 435 SVs from 55 studies. See in: genome view
Variant Region Placement Information
Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
---|---|---|---|---|---|---|---|---|---|
nsv5844611 | Submitted genomic | GRCh38 (hg38) | Primary Assembly | NC_000006.12 | Chr6 | 32,036,849 | 32,040,410 | ||
nsv5844611 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000006.11 | Chr6 | 32,004,626 | 32,008,187 |
Variant Call Information
Variant Call ID | Type | Method | Analysis | Copy number |
---|---|---|---|---|
nssv17505240 | copy number variation | Sequencing | Sequence alignment | 0 |
nssv17505241 | copy number variation | Sequencing | Sequence alignment | 2 |
nssv17505242 | copy number variation | Sequencing | Sequence alignment | 3 |
Variant Call Placement Information
Variant Call ID | Placement Type | Score | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
---|---|---|---|---|---|---|---|---|
nssv17505240 | Submitted genomic | GRCh38 (hg38) | NC_000006.12 | Chr6 | 32,036,849 | 32,040,410 | ||
nssv17505241 | Submitted genomic | GRCh38 (hg38) | NC_000006.12 | Chr6 | 32,036,849 | 32,040,410 | ||
nssv17505242 | Submitted genomic | GRCh38 (hg38) | NC_000006.12 | Chr6 | 32,036,849 | 32,040,410 | ||
nssv17505240 | Remapped | Perfect | GRCh37.p13 | First Pass | NC_000006.11 | Chr6 | 32,004,626 | 32,008,187 |
nssv17505241 | Remapped | Perfect | GRCh37.p13 | First Pass | NC_000006.11 | Chr6 | 32,004,626 | 32,008,187 |
nssv17505242 | Remapped | Perfect | GRCh37.p13 | First Pass | NC_000006.11 | Chr6 | 32,004,626 | 32,008,187 |