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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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| nstd233 | nssv18830931 | copy number loss | Sequencing | Curated | No | LLDD008.3 | GRCh37.p13 | NC_000017.10 | 17 | 59529098 | 60599347 | Remapped | 1 | ||||||||
| nstd233 | nssv18830931 | copy number loss | Sequencing | Curated | No | LLDD008.3 | GRCh37.p13 | NC_000017.10 | 17 | 59529098 | 60599347 | Remapped | 1 | ||||||||
| nstd233 | nssv18830931 | copy number loss | Sequencing | Curated | No | LLDD008.3 | GRCh38 (hg38) | NC_000017.11 | 17 | 61451737 | 62521986 | Submitted genomic | |||||||||
| nstd233 | nssv18830931 | copy number loss | Sequencing | Curated | No | LLDD008.3 | GRCh38 (hg38) | NC_000017.11 | 17 | 61451737 | 62521986 | Submitted genomic |