nsv436855
- Organism: Homo sapiens
- Study:nstd16 (Korbel et al. 2007)
- Variant Type:insertion
- Method Type:Sequencing
- Submitted on:NCBI36 (hg18)
- Variant Calls:1
- Validation:Yes
- Clinical Assertions: No
- Region Size:32,074
- Description:Unmated-Insertion
- Publication(s):Korbel et al. 2007
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: 577 SVs from 83 studies. See in: genome view
Overlapping variant regions from other studies: 577 SVs from 83 studies. See in: genome view
Overlapping variant regions from other studies: 196 SVs from 26 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Outer Start | Outer Stop |
|---|---|---|---|---|---|---|---|---|---|
| nsv436855 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000019.10 | Chr19 | 52,823,709 | 52,855,782 |
| nsv436855 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000019.9 | Chr19 | 53,326,962 | 53,359,035 |
| nsv436855 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000019.8 | Chr19 | 58,018,774 | 58,050,847 |
Variant Call Information
| Variant Call ID | Type | Sample ID | Method | Analysis | Other Calls in this Sample and Study |
|---|---|---|---|---|---|
| nssv465691 | insertion | SAMN00001583 | Sequencing | Paired-end mapping | 822 |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Outer Start | Outer Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv465691 | Remapped | Perfect | NC_000019.10:g.(52 823709_?)_(?_52855 782)ins? | GRCh38.p12 | First Pass | NC_000019.10 | Chr19 | 52,823,709 | 52,855,782 |
| nssv465691 | Remapped | Perfect | NC_000019.9:g.(533 26962_?)_(?_533590 35)ins? | GRCh37.p13 | First Pass | NC_000019.9 | Chr19 | 53,326,962 | 53,359,035 |
| nssv465691 | Submitted genomic | NC_000019.8:g.(580 18774_?)_(?_580508 47)ins(0_?) | NCBI36 (hg18) | NC_000019.8 | Chr19 | 58,018,774 | 58,050,847 |
Validation Information
| Variant Call ID | Experiment ID | Sample ID | Method | Analysis | Result |
|---|---|---|---|---|---|
| nssv465691 | 4 | SAMN00001583 | PCR | Manual observation | Pass |