nsv819556
- Organism: Homo sapiens
- Study:nstd43 (Kim et al. 2009)
- Variant Type:insertion
- Method Type:Sequencing
- Submitted on:NCBI36 (hg18)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:357
- Publication(s):Kim et al. 2009
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: 166 SVs from 35 studies. See in: genome view
Overlapping variant regions from other studies: 166 SVs from 35 studies. See in: genome view
Overlapping variant regions from other studies: 31 SVs from 11 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv819556 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000020.11 | Chr20 | 44,404,723 | 44,405,079 |
| nsv819556 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000020.10 | Chr20 | 43,033,363 | 43,033,719 |
| nsv819556 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000020.9 | Chr20 | 42,466,777 | 42,467,133 |
Variant Call Information
| Variant Call ID | Type | Sample ID | Method | Analysis | Other Calls in this Sample and Study |
|---|---|---|---|---|---|
| nssv1418903 | insertion | SAMN00002681 | Sequencing | Paired-end mapping | 1,333 |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Outer Start | Outer Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv1418903 | Remapped | Perfect | NC_000020.11:g.(44 404723_?)_(?_44405 079)ins923 | GRCh38.p12 | First Pass | NC_000020.11 | Chr20 | 44,404,723 | 44,405,079 |
| nssv1418903 | Remapped | Perfect | NC_000020.10:g.(43 033363_?)_(?_43033 719)ins923 | GRCh37.p13 | First Pass | NC_000020.10 | Chr20 | 43,033,363 | 43,033,719 |
| nssv1418903 | Submitted genomic | NC_000020.9:g.(424 66777_?)_(?_424671 33)ins923 | NCBI36 (hg18) | NC_000020.9 | Chr20 | 42,466,777 | 42,467,133 |