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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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| nstd181 | nsv4578340 | copy number variation | No | GRCh37 (hg19) | NC_000002.11 | 2 | 44664433 | 44846960 | Submitted genomic | ||||||||||||
| nstd181 | nsv4578340 | copy number variation | No | GRCh37 (hg19) | NC_000002.11 | 2 | 44664433 | 44846960 | Submitted genomic | ||||||||||||
| nstd181 | nsv4578340 | copy number variation | No | GRCh38.p12 | NC_000002.12 | 2 | 44437294 | 44619821 | Remapped | 1 |