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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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| estd48 | esv33998 | inversion | No | GRCh37.p13 | NC_000017.10 | 17 | 40557196 | 40557196 | 41455196 | 41455196 | Remapped | 0.898 | |||||||||
| estd48 | esv33998 | inversion | No | GRCh37.p13 | NC_000017.10 | 17 | 40557196 | 40557196 | 41455196 | 41455196 | Remapped | 0.898 | |||||||||
| estd48 | esv33998 | inversion | No | GRCh38.p12 | NC_000017.11 | 17 | 42405178 | 42405178 | 43377828 | 43377828 | Remapped | 0.97265 | |||||||||
| estd48 | esv33998 | inversion | No | NCBI34 (hg16) | NC_000017.8 | 17 | 40930361 | 41030361 | 41830361 | 41930361 | Submitted genomic |