nsv6112763
- Organism: Homo sapiens
- Study:nstd102 (Clinical Structural Variants)
- Variant Type:copy number variation
- Method Type:Multiple
- Submitted on:GRCh37
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: Yes
- Region Size:7,497,821
- Description:GRCh37/hg19 12p13.33-13.31(chr12:189145-7730395)x3 AND not provided
- Genome View
- Variant Region Details and Evidence
- Validation Information
- Clinical Assertions
- Genotype Information
Genome View
Select assembly:Overlapping variant regions from other studies: 25097 SVs from 126 studies. See in: genome view
Overlapping variant regions from other studies: 24939 SVs from 126 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nsv6112763 | Remapped | Good | GRCh38.p12 | Primary Assembly | First Pass | NC_000012.12 | Chr12 | 79,979 | 7,577,799 |
| nsv6112763 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000012.11 | Chr12 | 189,145 | 7,730,395 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis | Subject Phenotype | Clinical Interpretation | Source of Interpretation | ClinVar ID | Copy number |
|---|---|---|---|---|---|---|---|---|
| nssv17649928 | copy number gain | Multiple | Multiple | not provided | Pathogenic | ClinVar | RCV001537906.4, VCV001180524.4 | 3 |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv17649928 | Remapped | Good | NC_000012.12:g.799 79_7577799dup | GRCh38.p12 | First Pass | NC_000012.12 | Chr12 | 79,979 | 7,577,799 |
| nssv17649928 | Submitted genomic | NC_000012.11:g.189 145_7730395dup | GRCh37 (hg19) | NC_000012.11 | Chr12 | 189,145 | 7,730,395 |
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 | Copy number |
|---|---|---|---|---|---|---|---|---|
| nssv17649928 | GRCh37: NC_000012.11:g.189145_7730395dup | copy number gain | unknown | not provided | Pathogenic | ClinVar | RCV001537906.4, VCV001180524.4 | 3 |