nsv4674980
- 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:725,885
- Description:GRCh37/hg19 17q21.31(chr17:41399892-42125780)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: 2534 SVs from 94 studies. See in: genome view
Overlapping variant regions from other studies: 2560 SVs from 94 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv4674980 | Remapped | Good | GRCh38.p12 | Primary Assembly | First Pass | NC_000017.11 | Chr17 | 43,322,528 | 44,048,412 |
| nsv4674980 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000017.10 | Chr17 | 41,399,892 | 42,125,780 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis | Subject Phenotype | Clinical Interpretation | Source of Interpretation | ClinVar ID | Copy number |
|---|---|---|---|---|---|---|---|---|
| nssv16207327 | copy number gain | Multiple | Multiple | not provided | Uncertain significance | ClinVar | RCV001006903.1, VCV000815937.1 | 3 |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv16207327 | Remapped | Good | NC_000017.11:g.(?_ 43322528)_(4404841 2_?)dup | GRCh38.p12 | First Pass | NC_000017.11 | Chr17 | 43,322,528 | 44,048,412 |
| nssv16207327 | Submitted genomic | NC_000017.10:g.(?_ 41399892)_(4212578 0_?)dup | GRCh37 (hg19) | NC_000017.10 | Chr17 | 41,399,892 | 42,125,780 |
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 |
|---|---|---|---|---|---|---|---|---|
| nssv16207327 | GRCh37: NC_000017.10:g.(?_41399892)_(42125780_?)dup | copy number gain | germline | not provided | Uncertain significance | ClinVar | RCV001006903.1, VCV000815937.1 | 3 |