nsv955099
- 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:136
- 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: 125 SVs from 27 studies. See in: genome view
Overlapping variant regions from other studies: 125 SVs from 27 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv955099 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000002.12 | Chr2 | 209,903,538 | 209,903,673 |
| nsv955099 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000002.11 | Chr2 | 210,768,262 | 210,768,397 |
Variant Call Information
| Variant Call ID | Type | Sample ID | Method | Analysis | Other Calls in this Sample and Study |
|---|---|---|---|---|---|
| nssv3003970 | 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 |
|---|---|---|---|---|---|---|---|---|---|
| nssv3003970 | Remapped | Perfect | NC_000002.12:g.(20 9903538_?)_(?_2099 03673)ins? | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 209,903,538 | 209,903,673 |
| nssv3003970 | Submitted genomic | NC_000002.11:g.(21 0768262_?)_(?_2107 68397)ins(0_?) | GRCh37 (hg19) | NC_000002.11 | Chr2 | 210,768,262 | 210,768,397 |