nsv3066915
- Organism: Homo sapiens
- Study:nstd140 (Fan et al. 2017)
- Variant Type:insertion
- Method Type:Sequencing
- Submitted on:GRCh37 (hg19)
- Variant is Defined by:KY429496
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:1
- Publication(s):Fan et al. 2017
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: 122 SVs from 37 studies. See in: genome view
Overlapping variant regions from other studies: 2 SVs from 2 studies. See in: genome view
Overlapping variant regions from other studies: 122 SVs from 37 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nsv3066915 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000007.14 | Chr7 | 99,219,898 | 99,219,898 |
| nsv3066915 | Remapped | Perfect | GRCh38.p12 | PATCHES | Second Pass | NW_017852929.1 | Chr7|NW_01 7852929.1 | 133,221 | 133,221 |
| nsv3066915 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000007.13 | Chr7 | 98,817,521 | 98,817,521 |
Variant Call Information
| Variant Call ID | Type | Sample ID | Method | Analysis | Other Calls in this Sample and Study |
|---|---|---|---|---|---|
| nssv14035861 | insertion | CHM1 | Sequencing | Local sequence assembly | 7,551 |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv14035861 | Remapped | Perfect | NW_017852929.1:g.1 33221_133222ins? | GRCh38.p12 | Second Pass | NW_017852929.1 | Chr7|NW_01 7852929.1 | 133,221 | 133,221 |
| nssv14035861 | Remapped | Perfect | NC_000007.14:g.992 19898_99219899ins? | GRCh38.p12 | First Pass | NC_000007.14 | Chr7 | 99,219,898 | 99,219,898 |
| nssv14035861 | Submitted genomic | NC_000007.13:g.988 17521_98817522ins? | GRCh37 (hg19) | NC_000007.13 | Chr7 | 98,817,521 | 98,817,521 |