nsv818624
- Organism: Homo sapiens
- Study:nstd64 (Wang et al. 2007)
- Variant Type:copy number variation
- Method Type:SNP array
- Submitted on:NCBI35 (hg17)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:62,246
- Publication(s):Wang et al. 2007
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: 287 SVs from 40 studies. See in: genome view
Overlapping variant regions from other studies: 287 SVs from 40 studies. See in: genome view
Overlapping variant regions from other studies: 19 SVs from 4 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 |
---|---|---|---|---|---|---|---|---|---|
nsv818624 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000008.11 | Chr8 | 49,970,270 | 50,032,515 |
nsv818624 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000008.10 | Chr8 | 50,882,830 | 50,945,075 |
nsv818624 | Submitted genomic | NCBI35 (hg17) | Primary Assembly | NC_000008.9 | Chr8 | 51,045,383 | 51,107,628 |
Variant Call Information
Variant Call Placement Information
Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
---|---|---|---|---|---|---|---|---|---|
nssv1418295 | Remapped | Perfect | NC_000008.11:g.(?_ 49970270)_(5003251 5_?)del | GRCh38.p12 | First Pass | NC_000008.11 | Chr8 | 49,970,270 | 50,032,515 |
nssv1418295 | Remapped | Perfect | NC_000008.10:g.(?_ 50882830)_(5094507 5_?)del | GRCh37.p13 | First Pass | NC_000008.10 | Chr8 | 50,882,830 | 50,945,075 |
nssv1418295 | Submitted genomic | NC_000008.9:g.(?_5 1045383)_(51107628 _?)del | NCBI35 (hg17) | NC_000008.9 | Chr8 | 51,045,383 | 51,107,628 |