nsv1067821
- 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:1,360,107
- 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: 3594 SVs from 102 studies. See in: genome view
Overlapping variant regions from other studies: 3594 SVs from 102 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| nsv1067821 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000002.12 | Chr2 | 75,217,802 | 75,217,846 | 76,577,864 | 76,577,908 |
| nsv1067821 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000002.11 | Chr2 | 75,444,928 | 75,444,972 | 76,804,990 | 76,805,034 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis |
|---|---|---|---|
| nssv3761524 | duplication | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| nssv3761524 | Remapped | Perfect | NC_000002.12:g.(75 217802_75217846)_( 76577864_76577908) dup | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 75,217,802 | 75,217,846 | 76,577,864 | 76,577,908 |
| nssv3761524 | Submitted genomic | NC_000002.11:g.(75 444928_75444972)_( 76804990_76805034) dup | GRCh37 (hg19) | NC_000002.11 | Chr2 | 75,444,928 | 75,444,972 | 76,804,990 | 76,805,034 |