nsv819929
- 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:357,101
- 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: 1432 SVs from 75 studies. See in: genome view
Overlapping variant regions from other studies: 1432 SVs from 75 studies. See in: genome view
Overlapping variant regions from other studies: 639 SVs from 26 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv819929 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000016.10 | Chr16 | 70,812,024 | 71,169,124 |
| nsv819929 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000016.9 | Chr16 | 70,845,927 | 71,203,027 |
| nsv819929 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000016.8 | Chr16 | 69,403,428 | 69,760,528 |
Variant Call Information
| Variant Call ID | Type | Sample ID | Method | Analysis | Other Calls in this Sample and Study |
|---|---|---|---|---|---|
| nssv1418917 | 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 |
|---|---|---|---|---|---|---|---|---|---|
| nssv1418917 | Remapped | Perfect | NC_000016.10:g.(70 812024_?)_(?_71169 124)ins? | GRCh38.p12 | First Pass | NC_000016.10 | Chr16 | 70,812,024 | 71,169,124 |
| nssv1418917 | Remapped | Perfect | NC_000016.9:g.(708 45927_?)_(?_712030 27)ins? | GRCh37.p13 | First Pass | NC_000016.9 | Chr16 | 70,845,927 | 71,203,027 |
| nssv1418917 | Submitted genomic | NC_000016.8:g.(694 03428_?)_(?_697605 28)ins(0_?) | NCBI36 (hg18) | NC_000016.8 | Chr16 | 69,403,428 | 69,760,528 |