nsv959686
- 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:82,742
- 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: 348 SVs from 59 studies. See in: genome view
Overlapping variant regions from other studies: 348 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv959686 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000006.12 | Chr6 | 151,009,817 | 151,092,558 |
| nsv959686 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000006.11 | Chr6 | 151,330,953 | 151,413,694 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis |
|---|---|---|---|
| nssv3020889 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| nssv3020889 | Remapped | Perfect | NC_000006.12:g.(15 0972060_150972060) _(151305745_151305 745)del | GRCh38.p12 | First Pass | NC_000006.12 | Chr6 | 150,972,060 | 150,972,060 | 151,305,745 | 151,305,745 |
| nssv3020889 | Submitted genomic | NC_000006.11:g.(15 1293196_151330953) _(151413694_151626 880)del | GRCh37 (hg19) | NC_000006.11 | Chr6 | 151,293,196 | 151,330,953 | 151,413,694 | 151,626,880 |