nsv4457130
- 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:2,571,159
- Description:GRCh37/hg19 7q36.1(chr7:149968222-152539376)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: 8921 SVs from 110 studies. See in: genome view
Overlapping variant regions from other studies: 8958 SVs from 110 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv4457130 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000007.14 | Chr7 | 150,271,133 | 152,842,291 |
| nsv4457130 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000007.13 | Chr7 | 149,968,222 | 152,539,376 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis | Subject Phenotype | Clinical Interpretation | Source of Interpretation | ClinVar ID | Copy number |
|---|---|---|---|---|---|---|---|---|
| nssv15772407 | copy number gain | Multiple | Multiple | not provided | Uncertain significance | ClinVar | RCV000847582.2, VCV000686874.2 | 3 |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv15772407 | Remapped | Perfect | NC_000007.14:g.(?_ 150271133)_(152842 291_?)dup | GRCh38.p12 | First Pass | NC_000007.14 | Chr7 | 150,271,133 | 152,842,291 |
| nssv15772407 | Submitted genomic | NC_000007.13:g.(?_ 149968222)_(152539 376_?)dup | GRCh37 (hg19) | NC_000007.13 | Chr7 | 149,968,222 | 152,539,376 |
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 |
|---|---|---|---|---|---|---|---|---|
| nssv15772407 | GRCh37: NC_000007.13:g.(?_149968222)_(152539376_?)dup | copy number gain | unknown | not provided | Uncertain significance | ClinVar | RCV000847582.2, VCV000686874.2 | 3 |