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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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| nstd154 | nsv3167734 | copy number variation | No | GRCh37.p13 | NC_000009.11 | 9 | 136127801 | 136133621 | Remapped | 1.00069 | |||||||||||
| nstd154 | nsv3167734 | copy number variation | No | GRCh37.p13 | NW_003315925.1 | 9|NW_003315925.1 | 78373 | 84324 | Remapped | 1.02321 | |||||||||||
| nstd154 | nsv3167734 | copy number variation | No | GRCh37.p13 | NC_000009.11 | 9 | 136127801 | 136133621 | Remapped | 1.00069 | |||||||||||
| nstd154 | nsv3167734 | copy number variation | No | GRCh37.p13 | NW_003315925.1 | 9|NW_003315925.1 | 78373 | 84324 | Remapped | 1.02321 | |||||||||||
| nstd154 | nsv3167734 | copy number variation | No | GRCh38 (hg38) | NC_000009.12 | 9 | 133252414 | 133258230 | Submitted genomic | ||||||||||||
| nstd154 | nsv3167734 | copy number variation | No | GRCh38 (hg38) | NC_000009.12 | 9 | 133252414 | 133258230 | Submitted genomic |