nsv1067814
- Organism: Homo sapiens
- Study:nstd98 (Campbell et al. 2014b)
- Variant Type:copy number variation
- Method Type:Sequencing
- Submitted on:GRCh37 (hg19)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:189,174
- Publication(s):Campbell et al. 2014
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: 678 SVs from 61 studies. See in: genome view
Overlapping variant regions from other studies: 678 SVs from 61 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Outer Start | Inner Start | Inner Stop | Outer Stop |
|---|---|---|---|---|---|---|---|---|---|---|---|
| nsv1067814 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000011.10 | Chr11 | 130,564,899 | 130,564,950 | 130,754,020 | 130,754,072 |
| nsv1067814 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000011.9 | Chr11 | 130,434,794 | 130,434,845 | 130,623,915 | 130,623,967 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis |
|---|---|---|---|
| nssv3761534 | deletion | Sequencing | Sequence alignment |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Outer Start | Inner Start | Inner Stop | Outer Stop |
|---|---|---|---|---|---|---|---|---|---|---|---|
| nssv3761534 | Remapped | Perfect | NC_000011.10:g.(13 0564899_130564950) _(130754020_130754 072)del | GRCh38.p12 | First Pass | NC_000011.10 | Chr11 | 130,564,899 | 130,564,950 | 130,754,020 | 130,754,072 |
| nssv3761534 | Submitted genomic | NC_000011.9:g.(130 434794_130434845)_ (130623915_1306239 67)del | GRCh37 (hg19) | NC_000011.9 | Chr11 | 130,434,794 | 130,434,845 | 130,623,915 | 130,623,967 |