nsv959023
- 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:124,371
- 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: 373 SVs from 46 studies. See in: genome view
Overlapping variant regions from other studies: 373 SVs from 46 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv959023 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000003.12 | Chr3 | 58,008,563 | 58,132,933 |
| nsv959023 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000003.11 | Chr3 | 57,994,290 | 58,118,660 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis |
|---|---|---|---|
| nssv3020789 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| nssv3020789 | Remapped | Perfect | NC_000003.12:g.(57 927390_58008563)_( 58132933_58134614) del | GRCh38.p12 | First Pass | NC_000003.12 | Chr3 | 57,927,390 | 58,008,563 | 58,132,933 | 58,134,614 |
| nssv3020789 | Submitted genomic | NC_000003.11:g.(57 913117_57994290)_( 58118660_58120341) del | GRCh37 (hg19) | NC_000003.11 | Chr3 | 57,913,117 | 57,994,290 | 58,118,660 | 58,120,341 |