nsv959353
- 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:42,508
- 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: 132 SVs from 30 studies. See in: genome view
Overlapping variant regions from other studies: 132 SVs from 30 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv959353 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000003.12 | Chr3 | 102,435,113 | 102,477,620 |
| nsv959353 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000003.11 | Chr3 | 102,153,957 | 102,196,464 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis |
|---|---|---|---|
| nssv3021149 | deletion | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| nssv3021149 | Remapped | Perfect | NC_000003.12:g.(10 1859373_102435113) _(102477620_105367 407)del | GRCh38.p12 | First Pass | NC_000003.12 | Chr3 | 101,859,373 | 102,435,113 | 102,477,620 | 105,367,407 |
| nssv3021149 | Submitted genomic | NC_000003.11:g.(10 1578217_102153957) _(102196464_105086 251)del | GRCh37 (hg19) | NC_000003.11 | Chr3 | 101,578,217 | 102,153,957 | 102,196,464 | 105,086,251 |