nsv3971563
- Organism: Homo sapiens
- Study:nstd168 (Levy-Sakin et al. 2019)
- Variant Type:translocation
- Method Type:Optical mapping
- Submitted on:GRCh38 (hg38)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:1
- Publication(s):Levy-Sakin et al. 2019
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: 109 SVs from 20 studies. See in: genome view
Overlapping variant regions from other studies: 107 SVs from 20 studies. See in: genome view
Overlapping variant regions from other studies: 109 SVs from 20 studies. See in: genome view
Overlapping variant regions from other studies: 107 SVs from 20 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop | strand |
|---|---|---|---|---|---|---|---|---|---|---|
| nsv3971563 | Submitted genomic | GRCh38 (hg38) | Primary Assembly | NC_000003.12 | Chr3 | 135,307,046 | 135,307,046 | + | ||
| nsv3971563 | Submitted genomic | GRCh38 (hg38) | Primary Assembly | NC_000012.12 | Chr12 | 125,372,923 | 125,372,923 | + | ||
| nsv3971563 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000003.11 | Chr3 | 135,025,888 | 135,025,888 | + |
| nsv3971563 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000012.11 | Chr12 | 125,857,469 | 125,857,469 | + |
Variant Call Information
| Variant Call ID | Type | Method | Analysis |
|---|---|---|---|
| nssv15220055 | interchromosomal translocation | Optical mapping | Optical mapping |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop | strand |
|---|---|---|---|---|---|---|---|---|---|
| nssv15220055 | Submitted genomic | GRCh38 (hg38) | NC_000003.12 | Chr3 | 135,307,046 | 135,307,046 | + | ||
| nssv15220055 | Submitted genomic | GRCh38 (hg38) | NC_000012.12 | Chr12 | 125,372,923 | 125,372,923 | + | ||
| nssv15220055 | Remapped | Perfect | GRCh37.p13 | First Pass | NC_000003.11 | Chr3 | 135,025,888 | 135,025,888 | + |
| nssv15220055 | Remapped | Perfect | GRCh37.p13 | First Pass | NC_000012.11 | Chr12 | 125,857,469 | 125,857,469 | + |