nsv6637737
- 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:692,589
- Description:GRCh37/hg19 12q21.1-21.2(chr12:75417920-76110508)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: 1610 SVs from 69 studies. See in: genome view
Overlapping variant regions from other studies: 1610 SVs from 69 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv6637737 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000012.12 | Chr12 | 75,024,140 | 75,716,728 |
| nsv6637737 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000012.11 | Chr12 | 75,417,920 | 76,110,508 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis | Subject Phenotype | Clinical Interpretation | Source of Interpretation | ClinVar ID | Copy number |
|---|---|---|---|---|---|---|---|---|
| nssv18330338 | copy number gain | Multiple | Multiple | not provided | Uncertain significance | ClinVar | RCV002474598.1, VCV001808753.1 | 3 |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv18330338 | Remapped | Perfect | NC_000012.12:g.(?_ 75024140)_(7571672 8_?)dup | GRCh38.p12 | First Pass | NC_000012.12 | Chr12 | 75,024,140 | 75,716,728 |
| nssv18330338 | Submitted genomic | NC_000012.11:g.(?_ 75417920)_(7611050 8_?)dup | GRCh37 (hg19) | NC_000012.11 | Chr12 | 75,417,920 | 76,110,508 |
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 |
|---|---|---|---|---|---|---|---|---|
| nssv18330338 | GRCh37: NC_000012.11:g.(?_75417920)_(76110508_?)dup | copy number gain | unknown | not provided | Uncertain significance | ClinVar | RCV002474598.1, VCV001808753.1 | 3 |