nsv820356
- Organism: Homo sapiens
- Study:nstd65 (Ju et al. 2010)
- Variant Type:copy number variation
- Method Type:Sequencing
- Submitted on:NCBI36 (hg18)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:15,085
- Publication(s):Ju et al. 2010
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: 1145 SVs from 71 studies. See in: genome view
Overlapping variant regions from other studies: 1145 SVs from 71 studies. See in: genome view
Overlapping variant regions from other studies: 281 SVs from 21 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nsv820356 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000004.12 | Chr4 | 186,958,952 | 186,974,036 |
| nsv820356 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000004.11 | Chr4 | 187,880,106 | 187,895,190 |
| nsv820356 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000004.10 | Chr4 | 188,117,100 | 188,132,184 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv1420468 | Remapped | Perfect | NC_000004.12:g.(?_ 186958952)_(186974 036_?)del | GRCh38.p12 | First Pass | NC_000004.12 | Chr4 | 186,958,952 | 186,974,036 |
| nssv1420468 | Remapped | Perfect | NC_000004.11:g.(?_ 187880106)_(187895 190_?)del | GRCh37.p13 | First Pass | NC_000004.11 | Chr4 | 187,880,106 | 187,895,190 |
| nssv1420468 | Submitted genomic | NC_000004.10:g.(?_ 188117100)_(188132 184_?)del | NCBI36 (hg18) | NC_000004.10 | Chr4 | 188,117,100 | 188,132,184 |