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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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| nstd139 | nsv3067119 | copy number variation | No | GRCh37 (hg19) | NC_000015.9 | 15 | 43894500 | 43950000 | Submitted genomic | ||||||||||||
| nstd139 | nsv3067119 | copy number variation | No | GRCh37 (hg19) | NC_000015.9 | 15 | 43894500 | 43950000 | Submitted genomic | ||||||||||||
| nstd139 | nsv3067119 | copy number variation | No | GRCh38.p12 | NC_000015.10 | 15 | 43602302 | 43657802 | Remapped | 1 |