nsv4450583
- 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:66,397,404
- Description:GRCh37/hg19 1q25.3-44(chr1:182388773-249111240)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: 176967 SVs from 147 studies. See in: genome view
Overlapping variant regions from other studies: 176810 SVs from 147 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv4450583 | Remapped | Good | GRCh38.p12 | Primary Assembly | First Pass | NC_000001.11 | Chr1 | 182,419,638 | 248,817,041 |
| nsv4450583 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000001.10 | Chr1 | 182,388,773 | 249,111,240 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis | Subject Phenotype | Clinical Interpretation | Source of Interpretation | ClinVar ID | Copy number |
|---|---|---|---|---|---|---|---|---|
| nssv15777262 | copy number gain | Multiple | Multiple | not provided | Pathogenic | ClinVar | RCV000845852.2, VCV000685144.2 | 3 |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv15777262 | Remapped | Good | NC_000001.11:g.(?_ 182419638)_(248817 041_?)dup | GRCh38.p12 | First Pass | NC_000001.11 | Chr1 | 182,419,638 | 248,817,041 |
| nssv15777262 | Submitted genomic | NC_000001.10:g.(?_ 182388773)_(249111 240_?)dup | GRCh37 (hg19) | NC_000001.10 | Chr1 | 182,388,773 | 249,111,240 |
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 |
|---|---|---|---|---|---|---|---|---|
| nssv15777262 | GRCh37: NC_000001.10:g.(?_182388773)_(249111240_?)dup | copy number gain | unknown | not provided | Pathogenic | ClinVar | RCV000845852.2, VCV000685144.2 | 3 |