nsv3876412
- Organism: Homo sapiens
- Study:nstd102 (Clinical Structural Variants)
- Variant Type:copy number variation
- Method Type:Multiple
- Submitted on:GRCh37, GRCh38
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: Yes
- Region Size:21,359
- Description:Single allele AND Normal pregnancy
- Publication(s):Kasak et al. 2015
- Genome View
- Variant Region Details and Evidence
- Validation Information
- Clinical Assertions
- Genotype Information
Genome View
Select assembly:Overlapping variant regions from other studies: 177 SVs from 44 studies. See in: genome view
Overlapping variant regions from other studies: 177 SVs from 44 studies. See in: genome view
Variant Region Placement Information
Variant Region ID | Placement Type | Assembly | Assembly Unit | Sequence ID | Chr | Start | Stop |
---|---|---|---|---|---|---|---|
nsv3876412 | Submitted genomic | GRCh38 (hg38) | Primary Assembly | NC_000016.10 | Chr16 | 79,218,427 | 79,239,785 |
nsv3876412 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000016.9 | Chr16 | 79,252,324 | 79,273,682 |
Variant Call Information
Variant Call ID | Type | Method | Analysis | Subject Phenotype | Clinical Interpretation | Source of Interpretation | ClinVar ID |
---|---|---|---|---|---|---|---|
nssv15123623 | deletion | Multiple | Multiple | Normal pregnancy | not provided | ClinVar | RCV000161798.1, VCV000157372.1 |
Variant Call Placement Information
Variant Call ID | Placement Type | HGVS | Assembly | Sequence ID | Chr | Start | Stop |
---|---|---|---|---|---|---|---|
nssv15123623 | Submitted genomic | NC_000016.10:g.792 18427_79239785del | GRCh38 (hg38) | NC_000016.10 | Chr16 | 79,218,427 | 79,239,785 |
nssv15123623 | Submitted genomic | NC_000016.9:g.7925 2324_79273682del | GRCh37 (hg19) | NC_000016.9 | Chr16 | 79,252,324 | 79,273,682 |
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 |
---|---|---|---|---|---|---|---|
nssv15123623 | GRCh37: NC_000016.9:g.79252324_79273682del, GRCh38: NC_000016.10:g.79218427_79239785del | deletion | unknown | Normal pregnancy | not provided | ClinVar | RCV000161798.1, VCV000157372.1 |