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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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| nstd187 | nsv4684017 | copy number variation | No | GRCh37 (hg19) | NC_000008.10 | 8 | 6872895 | 6876338 | Submitted genomic | ||||||||||||
| nstd187 | nsv4684017 | copy number variation | No | GRCh37 (hg19) | NC_000008.10 | 8 | 6872895 | 6876338 | Submitted genomic | ||||||||||||
| nstd187 | nsv4684017 | copy number variation | No | GRCh38.p12 | NC_000008.11 | 8 | 7015373 | 7018816 | Remapped | 1 | |||||||||||
| nstd187 | nsv4684017 | copy number variation | No | GRCh38.p12 | NW_018654717.1 | 8|NW_018654717.1 | 410494 | 413940 | Remapped | 1.00087 |