nsv959382
- 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:68,252
- 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: 274 SVs from 49 studies. See in: genome view
Overlapping variant regions from other studies: 274 SVs from 49 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv959382 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000006.12 | Chr6 | 97,178,441 | 97,246,692 |
| nsv959382 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000006.11 | Chr6 | 97,626,317 | 97,694,568 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis |
|---|---|---|---|
| nssv3020881 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| nssv3020881 | Remapped | Perfect | NC_000006.12:g.(97 173224_97178441)_( 97246692_97254555) del | GRCh38.p12 | First Pass | NC_000006.12 | Chr6 | 97,173,224 | 97,178,441 | 97,246,692 | 97,254,555 |
| nssv3020881 | Submitted genomic | NC_000006.11:g.(97 621100_97626317)_( 97694568_97702431) del | GRCh37 (hg19) | NC_000006.11 | Chr6 | 97,621,100 | 97,626,317 | 97,694,568 | 97,702,431 |