nsv4456185
- 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:390,612
- Description:GRCh37/hg19 8q21.2(chr8:86346299-86836910)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: 1124 SVs from 89 studies. See in: genome view
Overlapping variant regions from other studies: 1139 SVs from 89 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv4456185 | Remapped | Pass | GRCh38.p12 | Primary Assembly | First Pass | NC_000008.11 | Chr8 | 85,434,070 | 85,824,681 |
| nsv4456185 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000008.10 | Chr8 | 86,346,299 | 86,836,910 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis | Subject Phenotype | Clinical Interpretation | Source of Interpretation | ClinVar ID | Copy number |
|---|---|---|---|---|---|---|---|---|
| nssv15776602 | copy number gain | Multiple | Multiple | not provided | Uncertain significance | ClinVar | RCV000849653.2, VCV000688962.2 | 3 |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv15776602 | Remapped | Pass | NC_000008.11:g.(?_ 85434070)_(8582468 1_?)dup | GRCh38.p12 | First Pass | NC_000008.11 | Chr8 | 85,434,070 | 85,824,681 |
| nssv15776602 | Submitted genomic | NC_000008.10:g.(?_ 86346299)_(8683691 0_?)dup | GRCh37 (hg19) | NC_000008.10 | Chr8 | 86,346,299 | 86,836,910 |
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 |
|---|---|---|---|---|---|---|---|---|
| nssv15776602 | GRCh37: NC_000008.10:g.(?_86346299)_(86836910_?)dup | copy number gain | unknown | not provided | Uncertain significance | ClinVar | RCV000849653.2, VCV000688962.2 | 3 |