nsv3067003
- Organism: Homo sapiens
- Study:nstd141 (Rambo-Martin et al. 2018)
- Variant Type:copy number variation
- Method Type:Oligo aCGH
- Submitted on:GRCh37 (hg19)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:22,207
- Publication(s):Rambo-Martin et al. 2018
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: 468 SVs from 53 studies. See in: genome view
Overlapping variant regions from other studies: 468 SVs from 53 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 |
---|---|---|---|---|---|---|---|---|---|
nsv3067003 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000021.9 | Chr21 | 18,685,877 | 18,708,083 |
nsv3067003 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000021.8 | Chr21 | 20,058,195 | 20,080,401 |
Variant Call Information
Variant Call ID | Type | Method | Analysis |
---|---|---|---|
nssv14038671 | copy number gain | Oligo aCGH | Probe signal intensity |
Variant Call Placement Information
Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
---|---|---|---|---|---|---|---|---|---|
nssv14038671 | Remapped | Perfect | NC_000021.9:g.(?_1 8685877)_(18708083 _?)dup | GRCh38.p12 | First Pass | NC_000021.9 | Chr21 | 18,685,877 | 18,708,083 |
nssv14038671 | Submitted genomic | NC_000021.8:g.(?_2 0058195)_(20080401 _?)dup | GRCh37 (hg19) | NC_000021.8 | Chr21 | 20,058,195 | 20,080,401 |