nsv433396
- Organism: Homo sapiens
- Study:nstd14 (Cooper et al. 2008)
- Variant Type:copy number variation
- Method Type:SNP array
- Submitted on:NCBI35 (hg17)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:21,523
- Publication(s):Cooper et al. 2008
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: 458 SVs from 72 studies. See in: genome view
Overlapping variant regions from other studies: 316 SVs from 51 studies. See in: genome view
Overlapping variant regions from other studies: 42 SVs from 11 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv433396 | Remapped | Perfect | GRCh38.p12 | ALT_REF_LOCI_1 | First Pass | NT_187576.1 | Chr8|NT_18 7576.1 | 501,806 | 523,328 |
| nsv433396 | Remapped | Perfect | GRCh37.p13 | PATCHES | First Pass | NW_003571042.1 | Chr8|NW_00 3571042.1 | 301,207 | 322,729 |
| nsv433396 | Submitted genomic | NCBI35 (hg17) | Primary Assembly | NC_000008.9 | Chr8 | 2,254,003 | 2,275,525 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv463277 | Remapped | Perfect | NT_187576.1:g.(?_5 01806)_(523328_?)d up | GRCh38.p12 | First Pass | NT_187576.1 | Chr8|NT_18 7576.1 | 501,806 | 523,328 |
| nssv463277 | Remapped | Perfect | NW_003571042.1:g.( ?_301207)_(322729_ ?)dup | GRCh37.p13 | First Pass | NW_003571042.1 | Chr8|NW_00 3571042.1 | 301,207 | 322,729 |
| nssv463277 | Submitted genomic | NC_000008.9:g.(?_2 254003)_(2275525_? )dup | NCBI35 (hg17) | NC_000008.9 | Chr8 | 2,254,003 | 2,275,525 |