nsv5570510
- Organism: Homo sapiens
- Study:nstd207 (Ebert et al. 2021)
- Variant Type:copy number variation
- Method Type:Sequencing
- Submitted on:GRCh38
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:51
- Publication(s):Ebert et al. 2021
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: 97 SVs from 32 studies. See in: genome view
Overlapping variant regions from other studies: 97 SVs from 32 studies. See in: genome view
Variant Region Placement Information
Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
---|---|---|---|---|---|---|---|---|---|
nsv5570510 | Submitted genomic | GRCh38 (hg38) | Primary Assembly | NC_000007.14 | Chr7 | 35,632,266 | 35,632,316 | ||
nsv5570510 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000007.13 | Chr7 | 35,671,876 | 35,671,926 |
Variant Call Information
Variant Call Placement Information
Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
---|---|---|---|---|---|---|---|---|---|
nssv17151019 | Submitted genomic | NC_000007.14:g.356 32266_35632316delC | GRCh38 (hg38) | NC_000007.14 | Chr7 | 35,632,266 | 35,632,316 | ||
nssv17151019 | Remapped | Perfect | NC_000007.13:g.356 71876_35671926delC | GRCh37.p13 | First Pass | NC_000007.13 | Chr7 | 35,671,876 | 35,671,926 |