nsv437048
- Organism: Homo sapiens
- Study:nstd17 (Conrad et al. 2005)
- Variant Type:copy number variation
- Method Type:SNP array
- Submitted on:NCBI34 (hg16)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:120,509
- Publication(s):Conrad et al. 2005
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: 736 SVs from 68 studies. See in: genome view
Overlapping variant regions from other studies: 736 SVs from 68 studies. See in: genome view
Overlapping variant regions from other studies: 3 SVs from 2 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Outer Start | Inner Start | Inner Stop | Outer Stop |
|---|---|---|---|---|---|---|---|---|---|---|---|
| nsv437048 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000008.11 | Chr8 | 14,715,712 | 14,777,603 | 14,833,416 | 14,836,220 |
| nsv437048 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000008.10 | Chr8 | 14,573,221 | 14,635,112 | 14,690,925 | 14,693,729 |
| nsv437048 | Submitted genomic | NCBI34 (hg16) | Primary Assembly | NC_000008.8 | Chr8 | 14,583,587 | 14,645,478 | 14,701,291 | 14,704,095 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Outer Start | Inner Start | Inner Stop | Outer Stop |
|---|---|---|---|---|---|---|---|---|---|---|---|
| nssv466929 | Remapped | Perfect | NC_000008.11:g.(14 715712_14777603)_( 14833416_14836220) del | GRCh38.p12 | First Pass | NC_000008.11 | Chr8 | 14,715,712 | 14,777,603 | 14,833,416 | 14,836,220 |
| nssv466929 | Remapped | Perfect | NC_000008.10:g.(14 573221_14635112)_( 14690925_14693729) del | GRCh37.p13 | First Pass | NC_000008.10 | Chr8 | 14,573,221 | 14,635,112 | 14,690,925 | 14,693,729 |
| nssv466929 | Submitted genomic | NC_000008.8:g.(145 83587_14645478)_(1 4701291_14704095)d el | NCBI34 (hg16) | NC_000008.8 | Chr8 | 14,583,587 | 14,645,478 | 14,701,291 | 14,704,095 |