nsv819669
- 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:50,501
- 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: 420 SVs from 30 studies. See in: genome view
Overlapping variant regions from other studies: 421 SVs from 30 studies. See in: genome view
Overlapping variant regions from other studies: 105 SVs from 8 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv819669 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000024.10 | ChrY | 21,495,751 | 21,546,251 |
| nsv819669 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000024.9 | ChrY | 23,657,637 | 23,708,137 |
| nsv819669 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000024.8 | ChrY | 22,067,025 | 22,117,525 |
Variant Call Information
| Variant Call ID | Type | Sample ID | Method | Analysis | Other Calls in this Sample and Study |
|---|---|---|---|---|---|
| nssv1418919 | 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 |
|---|---|---|---|---|---|---|---|---|---|
| nssv1418919 | Remapped | Perfect | NC_000024.10:g.(21 495751_?)_(?_21546 251)ins? | GRCh38.p12 | First Pass | NC_000024.10 | ChrY | 21,495,751 | 21,546,251 |
| nssv1418919 | Remapped | Perfect | NC_000024.9:g.(236 57637_?)_(?_237081 37)ins? | GRCh37.p13 | First Pass | NC_000024.9 | ChrY | 23,657,637 | 23,708,137 |
| nssv1418919 | Submitted genomic | NC_000024.8:g.(220 67025_?)_(?_221175 25)ins(0_?) | NCBI36 (hg18) | NC_000024.8 | ChrY | 22,067,025 | 22,117,525 |