nsv4432411
- Organism: Homo sapiens
- Study:nstd172 (Deng et al. 2019)
- Variant Type:copy number variation
- Method Type:Sequencing
- Submitted on:GRCh37 (hg19)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:34,000
- Publication(s):Deng 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: 588 SVs from 63 studies. See in: genome view
Overlapping variant regions from other studies: 588 SVs from 63 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nsv4432411 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000016.10 | Chr16 | 89,089,593 | 89,123,592 |
| nsv4432411 | Submitted genomic | GRCh37.p13 | Primary Assembly | NC_000016.9 | Chr16 | 89,156,001 | 89,190,000 |
Variant Call Information
| Variant Call ID | Type | Sample ID | Method | Analysis | Other Calls in this Sample and Study |
|---|---|---|---|---|---|
| nssv15750850 | duplication | SMI018 | Sequencing | Sequence alignment | 551 |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv15750850 | Remapped | Perfect | NC_000016.10:g.890 89593_89123592dup | GRCh38.p12 | First Pass | NC_000016.10 | Chr16 | 89,089,593 | 89,123,592 |
| nssv15750850 | Submitted genomic | NC_000016.9:g.8915 6001_89190000dup | GRCh37.p13 | NC_000016.9 | Chr16 | 89,156,001 | 89,190,000 |