nsv959628
- 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:122,722
- 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: 400 SVs from 53 studies. See in: genome view
Overlapping variant regions from other studies: 400 SVs from 53 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv959628 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000007.14 | Chr7 | 14,718,542 | 14,841,263 |
| nsv959628 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000007.13 | Chr7 | 14,758,167 | 14,880,888 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis |
|---|---|---|---|
| nssv3020678 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| nssv3020678 | Remapped | Perfect | NC_000007.14:g.(14 701730_14718542)_( 14841263_15201283) dup | GRCh38.p12 | First Pass | NC_000007.14 | Chr7 | 14,701,730 | 14,718,542 | 14,841,263 | 15,201,283 |
| nssv3020678 | Submitted genomic | NC_000007.13:g.(14 741355_14758167)_( 14880888_15240908) dup | GRCh37 (hg19) | NC_000007.13 | Chr7 | 14,741,355 | 14,758,167 | 14,880,888 | 15,240,908 |