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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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| nstd219 | nsv6290358 | copy number variation | No | GRCh37.p13 | NC_000011.9 | 11 | 5247419 | 5252321 | Remapped | 1 | |||||||||||
| nstd219 | nsv6290358 | copy number variation | No | GRCh37.p13 | NC_000011.9 | 11 | 5247419 | 5252321 | Remapped | 1 | |||||||||||
| nstd219 | nsv6290358 | copy number variation | No | GRCh38 (hg38) | NC_000011.10 | 11 | 5226189 | 5231091 | Submitted genomic | ||||||||||||
| nstd219 | nsv6290358 | copy number variation | No | GRCh38 (hg38) | NC_000011.10 | 11 | 5226189 | 5231091 | Submitted genomic |