nsv513753
- Organism: Homo sapiens
- Study:nstd50 (Arlt et al. 2011)
- Variant Type:insertion
- Method Type:Sequencing
- Submitted on:NCBI36 (hg18)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:6,358
- Publication(s):Arlt et al. 2011
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: 219 SVs from 59 studies. See in: genome view
Overlapping variant regions from other studies: 217 SVs from 59 studies. See in: genome view
Overlapping variant regions from other studies: 39 SVs from 16 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 |
---|---|---|---|---|---|---|---|---|---|
nsv513753 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000017.11 | Chr17 | 41,376,532 | 41,382,889 |
nsv513753 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000017.10 | Chr17 | 39,532,784 | 39,539,141 |
nsv513753 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000017.9 | Chr17 | 36,786,310 | 36,792,667 |
Variant Call Information
Variant Call ID | Type | Sample ID | Method | Analysis | Other Calls in this Sample and Study |
---|---|---|---|---|---|
nssv627005 | insertion | 1 | Sequencing | Paired-end mapping | 2,637 |
Variant Call Placement Information
Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Outer Start | Outer Stop |
---|---|---|---|---|---|---|---|---|---|
nssv627005 | Remapped | Perfect | NC_000017.11:g.(41 376532_?)_(?_41382 889)ins6358 | GRCh38.p12 | First Pass | NC_000017.11 | Chr17 | 41,376,532 | 41,382,889 |
nssv627005 | Remapped | Perfect | NC_000017.10:g.(39 532784_?)_(?_39539 141)ins6358 | GRCh37.p13 | First Pass | NC_000017.10 | Chr17 | 39,532,784 | 39,539,141 |
nssv627005 | Submitted genomic | NC_000017.9:g.(367 86310_?)_(?_367926 67)ins6358 | NCBI36 (hg18) | NC_000017.9 | Chr17 | 36,786,310 | 36,792,667 |