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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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| nstd191 | nssv16214889 | inversion | Sequencing | Sequence alignment | No | DMD001 | GRCh37.p13 | NC_000023.10 | X | 32933886 | 87244324 | Remapped | 0.98614 | ||||||||
| nstd191 | nssv16214889 | inversion | Sequencing | Sequence alignment | No | DMD001 | GRCh37.p13 | NC_000023.10 | X | 32933886 | 87244324 | Remapped | 0.98614 | ||||||||
| nstd191 | nssv16214889 | inversion | Sequencing | Sequence alignment | No | DMD001 | GRCh38 (hg38) | NC_000023.11 | X | 32915769 | 87989324 | Submitted genomic | |||||||||
| nstd191 | nssv16214889 | inversion | Sequencing | Sequence alignment | No | DMD001 | GRCh38 (hg38) | NC_000023.11 | X | 32915769 | 87989324 | Submitted genomic | |||||||||
| nstd191 | nsv4684016 | inversion | No | GRCh37.p13 | NC_000023.10 | X | 32933886 | 87244324 | Remapped | 0.98614 | |||||||||||
| nstd191 | nsv4684016 | inversion | No | GRCh37.p13 | NC_000023.10 | X | 32933886 | 87244324 | Remapped | 0.98614 | |||||||||||
| nstd191 | nsv4684016 | inversion | No | GRCh38 (hg38) | NC_000023.11 | X | 32915769 | 87989324 | Submitted genomic | ||||||||||||
| nstd191 | nsv4684016 | inversion | No | GRCh38 (hg38) | NC_000023.11 | X | 32915769 | 87989324 | Submitted genomic |