nsv3887291
- Organism: Homo sapiens
- Study:nstd102 (Clinical Structural Variants)
- Variant Type:copy number variation
- Method Type:Multiple
- Submitted on:GRCh37, GRCh38
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: Yes
- Region Size:61,976
- Description:Single allele AND Normal pregnancy
- Publication(s):Kasak et al. 2015
- Genome View
- Variant Region Details and Evidence
- Validation Information
- Clinical Assertions
- Genotype Information
Genome View
Select assembly:Overlapping variant regions from other studies: 228 SVs from 46 studies. See in: genome view
Overlapping variant regions from other studies: 228 SVs from 46 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Assembly | Assembly Unit | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|
| nsv3887291 | Submitted genomic | GRCh38 (hg38) | Primary Assembly | NC_000016.10 | Chr16 | 63,486,872 | 63,548,847 |
| nsv3887291 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000016.9 | Chr16 | 63,520,776 | 63,582,751 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis | Subject Phenotype | Clinical Interpretation | Source of Interpretation | ClinVar ID |
|---|---|---|---|---|---|---|---|
| nssv15123622 | deletion | Multiple | Multiple | Normal pregnancy | not provided | ClinVar | RCV000161795.1, VCV000157369.1 |
Variant Call Placement Information
| Variant Call ID | Placement Type | HGVS | Assembly | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|
| nssv15123622 | Submitted genomic | NC_000016.10:g.634 86872_63548847del | GRCh38 (hg38) | NC_000016.10 | Chr16 | 63,486,872 | 63,548,847 |
| nssv15123622 | Submitted genomic | NC_000016.9:g.6352 0776_63582751del | GRCh37 (hg19) | NC_000016.9 | Chr16 | 63,520,776 | 63,582,751 |
No validation data were submitted for this variant
Clinical Assertions
| Variant Call ID | HGVS | Type | Allele Origin | Subject Phenotype | Clinical Interpretation | Source of Interpretation | ClinVar ID |
|---|---|---|---|---|---|---|---|
| nssv15123622 | GRCh37: NC_000016.9:g.63520776_63582751del, GRCh38: NC_000016.10:g.63486872_63548847del | deletion | unknown | Normal pregnancy | not provided | ClinVar | RCV000161795.1, VCV000157369.1 |