nsv959440
- 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:71,832
- 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: 324 SVs from 34 studies. See in: genome view
Overlapping variant regions from other studies: 324 SVs from 34 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv959440 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000008.11 | Chr8 | 112,234,363 | 112,306,194 |
| nsv959440 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000008.10 | Chr8 | 113,246,592 | 113,318,423 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis |
|---|---|---|---|
| nssv3021085 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| nssv3021085 | Remapped | Perfect | NC_000008.11:g.(11 2231634_112234363) _(112306194_112310 976)dup | GRCh38.p12 | First Pass | NC_000008.11 | Chr8 | 112,231,634 | 112,234,363 | 112,306,194 | 112,310,976 |
| nssv3021085 | Submitted genomic | NC_000008.10:g.(11 3243863_113246592) _(113318423_113323 205)dup | GRCh37 (hg19) | NC_000008.10 | Chr8 | 113,243,863 | 113,246,592 | 113,318,423 | 113,323,205 |