nsv959017
- 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:50,862
- 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: 346 SVs from 64 studies. See in: genome view
Overlapping variant regions from other studies: 346 SVs from 64 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv959017 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000004.12 | Chr4 | 74,174,535 | 74,225,396 |
| nsv959017 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000004.11 | Chr4 | 75,040,252 | 75,091,113 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis |
|---|---|---|---|
| nssv3021382 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| nssv3021382 | Remapped | Perfect | NC_000004.12:g.(74 098924_74174535)_( 74225396_74281423) del | GRCh38.p12 | First Pass | NC_000004.12 | Chr4 | 74,098,924 | 74,174,535 | 74,225,396 | 74,281,423 |
| nssv3021382 | Submitted genomic | NC_000004.11:g.(74 964641_75040252)_( 75091113_75147140) del | GRCh37 (hg19) | NC_000004.11 | Chr4 | 74,964,641 | 75,040,252 | 75,091,113 | 75,147,140 |