nsv3055755
- Organism: Homo sapiens
- Study:nstd140 (Fan et al. 2017)
- Variant Type:copy number variation
- Method Type:Sequencing
- Submitted on:GRCh37 (hg19)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:8,493
- Publication(s):Fan et al. 2017
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: 494 SVs from 81 studies. See in: genome view
Overlapping variant regions from other studies: 494 SVs from 81 studies. See in: genome view
Variant Region Placement Information
Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
---|---|---|---|---|---|---|---|---|---|
nsv3055755 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000004.12 | Chr4 | 172,503,883 | 172,512,375 |
nsv3055755 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000004.11 | Chr4 | 173,425,034 | 173,433,526 |
Variant Call Information
Variant Call ID | Type | Sample ID | Method | Analysis | Other Calls in this Sample and Study |
---|---|---|---|---|---|
nssv14027726 | deletion | CHM1 | Sequencing | Local sequence assembly | 7,551 |
Variant Call Placement Information
Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
---|---|---|---|---|---|---|---|---|---|
nssv14027726 | Remapped | Perfect | NC_000004.12:g.172 503883_172512375de l | GRCh38.p12 | First Pass | NC_000004.12 | Chr4 | 172,503,883 | 172,512,375 |
nssv14027726 | Submitted genomic | NC_000004.11:g.173 425034_173433526de l | GRCh37 (hg19) | NC_000004.11 | Chr4 | 173,425,034 | 173,433,526 |