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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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| nstd180 | nssv16091660 | deletion | Sequencing | Sequence alignment | No | d128 | GRCh37.p13 | NC_000023.10 | X | 114141331 | 114141411 | Remapped | 1 | ||||||||
| nstd180 | nssv16091660 | deletion | Sequencing | Sequence alignment | No | d128 | GRCh37.p13 | NW_004070891.1 | X|NW_004070891.1 | 575570 | 575650 | Remapped | 1 | ||||||||
| nstd180 | nssv16091660 | deletion | Sequencing | Sequence alignment | No | d128 | GRCh37.p13 | NC_000023.10 | X | 114141331 | 114141411 | Remapped | 1 | ||||||||
| nstd180 | nssv16091660 | deletion | Sequencing | Sequence alignment | No | d128 | GRCh37.p13 | NW_004070891.1 | X|NW_004070891.1 | 575570 | 575650 | Remapped | 1 | ||||||||
| nstd180 | nssv16091660 | deletion | Sequencing | Sequence alignment | No | d128 | GRCh38 (hg38) | NC_000023.11 | X | 114906768 | 114906848 | Submitted genomic | |||||||||
| nstd180 | nssv16091660 | deletion | Sequencing | Sequence alignment | No | d128 | GRCh38 (hg38) | NC_000023.11 | X | 114906768 | 114906848 | Submitted genomic | |||||||||
| nstd180 | nsv4578236 | copy number variation | No | GRCh37.p13 | NC_000023.10 | X | 114141331 | 114141411 | Remapped | 1 | |||||||||||
| nstd180 | nsv4578236 | copy number variation | No | GRCh37.p13 | NW_004070891.1 | X|NW_004070891.1 | 575570 | 575650 | Remapped | 1 | |||||||||||
| nstd180 | nsv4578236 | copy number variation | No | GRCh37.p13 | NC_000023.10 | X | 114141331 | 114141411 | Remapped | 1 | |||||||||||
| nstd180 | nsv4578236 | copy number variation | No | GRCh37.p13 | NW_004070891.1 | X|NW_004070891.1 | 575570 | 575650 | Remapped | 1 | |||||||||||
| nstd180 | nsv4578236 | copy number variation | No | GRCh38 (hg38) | NC_000023.11 | X | 114906768 | 114906848 | Submitted genomic | ||||||||||||
| nstd180 | nsv4578236 | copy number variation | No | GRCh38 (hg38) | NC_000023.11 | X | 114906768 | 114906848 | Submitted genomic |