nsv4369995
- Organism: Homo sapiens
- Study:nstd173 (Zarrei et al. 2019)
- Variant Type:copy number variation
- Method Type:SNP array
- Submitted on:GRCh37 (hg19)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:44,203
- Publication(s):Zarrei et al. 2019
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: 622 SVs from 74 studies. See in: genome view
Overlapping variant regions from other studies: 622 SVs from 74 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv4369995 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000012.12 | Chr12 | 31,866,504 | 31,910,706 |
| nsv4369995 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000012.11 | Chr12 | 32,019,438 | 32,063,640 |
Variant Call Information
| Variant Call ID | Type | Sample ID | Method | Analysis | Other Calls in this Sample and Study |
|---|---|---|---|---|---|
| nssv15697617 | copy number gain | 170927 | SNP array | Genotyping | 19 |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv15697617 | Remapped | Perfect | NC_000012.12:g.(?_ 31866504)_(3191070 6_?)dup | GRCh38.p12 | First Pass | NC_000012.12 | Chr12 | 31,866,504 | 31,910,706 |
| nssv15697617 | Submitted genomic | NC_000012.11:g.(?_ 32019438)_(3206364 0_?)dup | GRCh37 (hg19) | NC_000012.11 | Chr12 | 32,019,438 | 32,063,640 |