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| Study ID | Variant ID | Variant Region type | Variant Call type | Sampleset ID | Method | Analysis ID | Validation | Variant samples | Subject phenotype | Clinical Interpretation | Assembly | Accession | Chr | Outer-Start | Start | Inner-Start | Inner-End | End | Outer-End | Placement Type | Remap Score |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| nstd222 | nsv6315588 | copy number variation | No | GRCh37.p13 | NC_000016.9 | 16 | 85986306 | 86727693 | Remapped | 1 | |||||||||||
| nstd222 | nsv6315588 | copy number variation | No | GRCh37.p13 | NC_000016.9 | 16 | 85986306 | 86727693 | Remapped | 1 | |||||||||||
| nstd222 | nsv6315588 | copy number variation | No | GRCh38 (hg38) | NC_000016.10 | 16 | 85952700 | 86694087 | Submitted genomic | ||||||||||||
| nstd222 | nsv6315588 | copy number variation | No | GRCh38 (hg38) | NC_000016.10 | 16 | 85952700 | 86694087 | Submitted genomic |