nsv955077
- 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:151
- 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: 170 SVs from 34 studies. See in: genome view
Overlapping variant regions from other studies: 170 SVs from 34 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv955077 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000002.12 | Chr2 | 119,444,557 | 119,444,707 |
| nsv955077 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000002.11 | Chr2 | 120,202,133 | 120,202,283 |
Variant Call Information
| Variant Call ID | Type | Sample ID | Method | Analysis | Other Calls in this Sample and Study |
|---|---|---|---|---|---|
| nssv3003884 | 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 |
|---|---|---|---|---|---|---|---|---|---|
| nssv3003884 | Remapped | Perfect | NC_000002.12:g.(11 9444557_?)_(?_1194 44707)ins? | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 119,444,557 | 119,444,707 |
| nssv3003884 | Submitted genomic | NC_000002.11:g.(12 0202133_?)_(?_1202 02283)ins(0_?) | GRCh37 (hg19) | NC_000002.11 | Chr2 | 120,202,133 | 120,202,283 |