nsv959316
- Organism: Homo sapiens
- Study:nstd86 (Poultney et al. 2013)
- Variant Type:copy number variation
- Method Type:Sequencing
- Submitted on:GRCh37 (hg19)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:91,783
- Publication(s):Poultney et al. 2013
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: 325 SVs from 59 studies. See in: genome view
Overlapping variant regions from other studies: 325 SVs from 59 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nsv959316 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000004.12 | Chr4 | 142,082,029 | 142,173,811 |
| nsv959316 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000004.11 | Chr4 | 143,003,182 | 143,094,964 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis |
|---|---|---|---|
| nssv3021862 | duplication | Sequencing | Read depth |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Outer Start | Inner Start | Inner Stop | Outer Stop |
|---|---|---|---|---|---|---|---|---|---|---|---|
| nssv3021862 | Remapped | Perfect | NC_000004.12:g.(14 2028916_142082029) _(142173811_142193 085)dup | GRCh38.p12 | First Pass | NC_000004.12 | Chr4 | 142,028,916 | 142,082,029 | 142,173,811 | 142,193,085 |
| nssv3021862 | Submitted genomic | NC_000004.11:g.(14 2950069_143003182) _(143094964_143114 238)dup | GRCh37 (hg19) | NC_000004.11 | Chr4 | 142,950,069 | 143,003,182 | 143,094,964 | 143,114,238 |