nsv959697
- 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:47,367
- 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: 260 SVs from 49 studies. See in: genome view
Overlapping variant regions from other studies: 260 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv959697 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000007.14 | Chr7 | 134,174,554 | 134,221,920 |
| nsv959697 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000007.13 | Chr7 | 133,859,306 | 133,906,672 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis |
|---|---|---|---|
| nssv3020632 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| nssv3020632 | Remapped | Perfect | NC_000007.14:g.(13 4163542_134174554) _(134221920_134247 554)del | GRCh38.p12 | First Pass | NC_000007.14 | Chr7 | 134,163,542 | 134,174,554 | 134,221,920 | 134,247,554 |
| nssv3020632 | Submitted genomic | NC_000007.13:g.(13 3848294_133859306) _(133906672_133932 306)del | GRCh37 (hg19) | NC_000007.13 | Chr7 | 133,848,294 | 133,859,306 | 133,906,672 | 133,932,306 |