nsv956714
- Organism: Homo sapiens
- Study:nstd73 (Dogan et al. 2014)
- Variant Type:insertion
- Method Type:Sequencing
- Submitted on:GRCh37 (hg19)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:153
- Publication(s):Dogan 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: 141 SVs from 35 studies. See in: genome view
Overlapping variant regions from other studies: 141 SVs from 35 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv956714 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000001.11 | Chr1 | 51,852,537 | 51,852,689 |
| nsv956714 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000001.10 | Chr1 | 52,318,209 | 52,318,361 |
Variant Call Information
| Variant Call ID | Type | Sample ID | Method | Analysis | Other Calls in this Sample and Study |
|---|---|---|---|---|---|
| nssv3000533 | insertion | SAMN01096093 | Sequencing | Paired-end mapping | 9,109 |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Outer Start | Outer Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv3000533 | Remapped | Perfect | NC_000001.11:g.(51 852537_?)_(?_51852 689)ins? | GRCh38.p12 | First Pass | NC_000001.11 | Chr1 | 51,852,537 | 51,852,689 |
| nssv3000533 | Submitted genomic | NC_000001.10:g.(52 318209_?)_(?_52318 361)ins(0_?) | GRCh37 (hg19) | NC_000001.10 | Chr1 | 52,318,209 | 52,318,361 |