nsv4674962
- 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:628,167
- Description:GRCh37/hg19 16p13.3(chr16:106988-735154)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: 5096 SVs from 110 studies. See in: genome view
Overlapping variant regions from other studies: 5098 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 |
|---|---|---|---|---|---|---|---|---|---|
| nsv4674962 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000016.10 | Chr16 | 56,988 | 685,154 |
| nsv4674962 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000016.9 | Chr16 | 106,988 | 735,154 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis | Subject Phenotype | Clinical Interpretation | Source of Interpretation | ClinVar ID | Copy number |
|---|---|---|---|---|---|---|---|---|
| nssv16207247 | copy number gain | Multiple | Multiple | not provided | Uncertain significance | ClinVar | RCV001006742.1, VCV000815767.1 | 3 |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv16207247 | Remapped | Perfect | NC_000016.10:g.(?_ 56988)_(685154_?)d up | GRCh38.p12 | First Pass | NC_000016.10 | Chr16 | 56,988 | 685,154 |
| nssv16207247 | Submitted genomic | NC_000016.9:g.(?_1 06988)_(735154_?)d up | GRCh37 (hg19) | NC_000016.9 | Chr16 | 106,988 | 735,154 |
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 |
|---|---|---|---|---|---|---|---|---|
| nssv16207247 | GRCh37: NC_000016.9:g.(?_106988)_(735154_?)dup | copy number gain | germline | not provided | Uncertain significance | ClinVar | RCV001006742.1, VCV000815767.1 | 3 |