nsv1067820
- Organism: Homo sapiens
- Study:nstd98 (Campbell et al. 2014b)
- Variant Type:copy number variation
- Method Type:Sequencing
- Submitted on:GRCh37 (hg19)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:1,051,353
- Publication(s):Campbell et al. 2014
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: 2584 SVs from 93 studies. See in: genome view
Overlapping variant regions from other studies: 2590 SVs from 93 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Outer Start | Inner Start | Inner Stop | Outer Stop |
|---|---|---|---|---|---|---|---|---|---|---|---|
| nsv1067820 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000001.11 | Chr1 | 221,977,225 | 221,977,279 | 223,028,523 | 223,028,577 |
| nsv1067820 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000001.10 | Chr1 | 222,150,567 | 222,150,621 | 223,201,865 | 223,201,919 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis |
|---|---|---|---|
| nssv3761523 | deletion | Sequencing | Sequence alignment |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Outer Start | Inner Start | Inner Stop | Outer Stop |
|---|---|---|---|---|---|---|---|---|---|---|---|
| nssv3761523 | Remapped | Perfect | NC_000001.11:g.(22 1977225_221977279) _(223028523_223028 577)del | GRCh38.p12 | First Pass | NC_000001.11 | Chr1 | 221,977,225 | 221,977,279 | 223,028,523 | 223,028,577 |
| nssv3761523 | Submitted genomic | NC_000001.10:g.(22 2150567_222150621) _(223201865_223201 919)del | GRCh37 (hg19) | NC_000001.10 | Chr1 | 222,150,567 | 222,150,621 | 223,201,865 | 223,201,919 |