nsv958895
- 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:225,847
- 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: 997 SVs from 77 studies. See in: genome view
Overlapping variant regions from other studies: 997 SVs from 77 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv958895 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000010.11 | Chr10 | 54,153,098 | 54,378,944 |
| nsv958895 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000010.10 | Chr10 | 55,912,858 | 56,138,704 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis |
|---|---|---|---|
| nssv3021627 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| nssv3021627 | Remapped | Perfect | NC_000010.11:g.(54 133009_54153098)_( 54378944_54527810) dup | GRCh38.p12 | First Pass | NC_000010.11 | Chr10 | 54,133,009 | 54,153,098 | 54,378,944 | 54,527,810 |
| nssv3021627 | Submitted genomic | NC_000010.10:g.(55 892769_55912858)_( 56138704_56287570) dup | GRCh37 (hg19) | NC_000010.10 | Chr10 | 55,892,769 | 55,912,858 | 56,138,704 | 56,287,570 |