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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 | nssv16214933 | copy number variation | qPCR | Probe signal intensity | No | HG02614 | GRCh38.p12 | NC_000008.11 | 8 | 7015373 | 7018816 | Remapped | 1 | ||||||||
| nstd187 | nssv16214934 | copy number variation | qPCR | Probe signal intensity | No | HG02116 | GRCh38.p12 | NC_000008.11 | 8 | 7015373 | 7018816 | Remapped | 1 | ||||||||
| nstd187 | nssv16214935 | copy number variation | qPCR | Probe signal intensity | No | HG02733 | GRCh38.p12 | NC_000008.11 | 8 | 7015373 | 7018816 | Remapped | 1 | ||||||||
| nstd187 | nssv16214936 | copy number variation | qPCR | Probe signal intensity | No | HG02586 | GRCh38.p12 | NC_000008.11 | 8 | 7015373 | 7018816 | Remapped | 1 | ||||||||
| nstd187 | nssv16214937 | copy number variation | qPCR | Probe signal intensity | No | HG02047 | GRCh38.p12 | NC_000008.11 | 8 | 7015373 | 7018816 | Remapped | 1 | ||||||||
| nstd187 | nssv16214938 | copy number variation | qPCR | Probe signal intensity | No | NA18602 | GRCh38.p12 | NC_000008.11 | 8 | 7015373 | 7018816 | Remapped | 1 | ||||||||
| nstd187 | nssv16214939 | copy number variation | qPCR | Probe signal intensity | No | NA18946 | GRCh38.p12 | NC_000008.11 | 8 | 7015373 | 7018816 | Remapped | 1 | ||||||||
| nstd187 | nssv16214940 | copy number variation | qPCR | Probe signal intensity | No | HG02817 | GRCh38.p12 | NC_000008.11 | 8 | 7015373 | 7018816 | Remapped | 1 | ||||||||
| nstd187 | nssv16214941 | copy number variation | qPCR | Probe signal intensity | No | NA19440 | GRCh38.p12 | NC_000008.11 | 8 | 7015373 | 7018816 | Remapped | 1 | ||||||||
| nstd187 | nssv16214942 | copy number variation | qPCR | Probe signal intensity | No | HG02799 | GRCh38.p12 | NC_000008.11 | 8 | 7015373 | 7018816 | Remapped | 1 | ||||||||
| nstd187 | nssv16214943 | copy number variation | qPCR | Probe signal intensity | No | HG02577 | GRCh38.p12 | NC_000008.11 | 8 | 7015373 | 7018816 | Remapped | 1 | ||||||||
| nstd187 | nssv16214944 | copy number variation | qPCR | Probe signal intensity | No | HG00475 | GRCh38.p12 | NC_000008.11 | 8 | 7015373 | 7018816 | Remapped | 1 | ||||||||
| nstd187 | nssv16214945 | copy number variation | qPCR | Probe signal intensity | No | HG02398 | GRCh38.p12 | NC_000008.11 | 8 | 7015373 | 7018816 | Remapped | 1 | ||||||||
| nstd187 | nssv16214946 | copy number variation | qPCR | Probe signal intensity | No | HG00096 | GRCh38.p12 | NC_000008.11 | 8 | 7015373 | 7018816 | Remapped | 1 | ||||||||
| nstd187 | nssv16214947 | copy number variation | qPCR | Probe signal intensity | No | HG02624 | GRCh38.p12 | NC_000008.11 | 8 | 7015373 | 7018816 | Remapped | 1 | ||||||||
| nstd187 | nssv16214948 | copy number variation | qPCR | Probe signal intensity | No | NA19376 | GRCh38.p12 | NC_000008.11 | 8 | 7015373 | 7018816 | Remapped | 1 | ||||||||
| nstd187 | nssv16214949 | copy number variation | qPCR | Probe signal intensity | No | HG02798 | GRCh38.p12 | NC_000008.11 | 8 | 7015373 | 7018816 | Remapped | 1 | ||||||||
| nstd187 | nssv16214950 | copy number variation | qPCR | Probe signal intensity | No | HG03246 | GRCh38.p12 | NC_000008.11 | 8 | 7015373 | 7018816 | Remapped | 1 | ||||||||
| nstd187 | nssv16214951 | copy number variation | qPCR | Probe signal intensity | No | NA18968 | GRCh38.p12 | NC_000008.11 | 8 | 7015373 | 7018816 | Remapped | 1 | ||||||||
| nstd187 | nssv16214952 | copy number variation | Sequencing | Read depth | No | NA20278 | GRCh38.p12 | NC_000008.11 | 8 | 7015373 | 7018816 | Remapped | 1 | ||||||||
| nstd187 | nssv16214953 | copy number variation | Sequencing | Read depth | No | HG03055 | GRCh38.p12 | NC_000008.11 | 8 | 7015373 | 7018816 | Remapped | 1 | ||||||||
| nstd187 | nssv16214954 | copy number variation | Sequencing | Read depth | No | NA18877 | GRCh38.p12 | NC_000008.11 | 8 | 7015373 | 7018816 | Remapped | 1 | ||||||||
| nstd187 | nssv16214955 | copy number variation | Sequencing | Read depth | No | NA20359 | GRCh38.p12 | NC_000008.11 | 8 | 7015373 | 7018816 | Remapped | 1 | ||||||||
| nstd187 | nssv16214956 | copy number variation | Sequencing | Read depth | No | HG03097 | GRCh38.p12 | NC_000008.11 | 8 | 7015373 | 7018816 | Remapped | 1 | ||||||||
| nstd187 | nssv16214957 | copy number variation | Sequencing | Read depth | No | NA18959 | GRCh38.p12 | NC_000008.11 | 8 | 7015373 | 7018816 | Remapped | 1 | ||||||||
| nstd187 | nssv16214958 | copy number variation | Sequencing | Read depth | No | HG02407 | GRCh38.p12 | NC_000008.11 | 8 | 7015373 | 7018816 | Remapped | 1 | ||||||||
| nstd187 | nssv16214959 | copy number variation | Sequencing | Read depth | No | HG02611 | GRCh38.p12 | NC_000008.11 | 8 | 7015373 | 7018816 | Remapped | 1 | ||||||||
| nstd187 | nssv16214960 | copy number variation | Sequencing | Read depth | No | HG02479 | GRCh38.p12 | NC_000008.11 | 8 | 7015373 | 7018816 | Remapped | 1 | ||||||||
| nstd187 | nssv16214961 | copy number variation | Sequencing | Read depth | No | HG02133 | GRCh38.p12 | NC_000008.11 | 8 | 7015373 | 7018816 | Remapped | 1 | ||||||||
| nstd187 | nssv16214962 | copy number variation | Sequencing | Read depth | No | HG03085 | GRCh38.p12 | NC_000008.11 | 8 | 7015373 | 7018816 | Remapped | 1 | ||||||||
| nstd187 | nssv16214963 | copy number variation | Sequencing | Read depth | No | HG01914 | GRCh38.p12 | NC_000008.11 | 8 | 7015373 | 7018816 | Remapped | 1 | ||||||||
| nstd187 | nssv16214964 | copy number variation | Sequencing | Read depth | No | HG03058 | GRCh38.p12 | NC_000008.11 | 8 | 7015373 | 7018816 | Remapped | 1 | ||||||||
| nstd187 | nssv16214965 | copy number variation | Sequencing | Read depth | No | HG02614 | GRCh38.p12 | NC_000008.11 | 8 | 7015373 | 7018816 | Remapped | 1 | ||||||||
| nstd187 | nssv16214966 | copy number variation | Sequencing | Read depth | No | HG02116 | GRCh38.p12 | NC_000008.11 | 8 | 7015373 | 7018816 | Remapped | 1 | ||||||||
| nstd187 | nssv16214967 | copy number variation | Sequencing | Read depth | No | HG02733 | GRCh38.p12 | NC_000008.11 | 8 | 7015373 | 7018816 | Remapped | 1 | ||||||||
| nstd187 | nssv16214968 | copy number variation | Sequencing | Read depth | No | HG02586 | GRCh38.p12 | NC_000008.11 | 8 | 7015373 | 7018816 | Remapped | 1 | ||||||||
| nstd187 | nssv16214969 | copy number variation | Sequencing | Read depth | No | HG02047 | GRCh38.p12 | NC_000008.11 | 8 | 7015373 | 7018816 | Remapped | 1 | ||||||||
| nstd187 | nssv16214970 | copy number variation | Sequencing | Read depth | No | NA18602 | GRCh38.p12 | NC_000008.11 | 8 | 7015373 | 7018816 | Remapped | 1 | ||||||||
| nstd187 | nssv16214971 | copy number variation | Sequencing | Read depth | No | NA18946 | GRCh38.p12 | NC_000008.11 | 8 | 7015373 | 7018816 | Remapped | 1 | ||||||||
| nstd187 | nssv16214972 | copy number variation | Sequencing | Read depth | No | HG02817 | GRCh38.p12 | NC_000008.11 | 8 | 7015373 | 7018816 | Remapped | 1 | ||||||||
| nstd187 | nssv16214973 | copy number variation | Sequencing | Read depth | No | NA19440 | GRCh38.p12 | NC_000008.11 | 8 | 7015373 | 7018816 | Remapped | 1 | ||||||||
| nstd187 | nssv16214974 | copy number variation | Sequencing | Read depth | No | HG02799 | GRCh38.p12 | NC_000008.11 | 8 | 7015373 | 7018816 | Remapped | 1 | ||||||||
| nstd187 | nssv16214975 | copy number variation | Sequencing | Read depth | No | HG02577 | GRCh38.p12 | NC_000008.11 | 8 | 7015373 | 7018816 | Remapped | 1 | ||||||||
| nstd187 | nssv16214976 | copy number variation | Sequencing | Read depth | No | HG00475 | GRCh38.p12 | NC_000008.11 | 8 | 7015373 | 7018816 | Remapped | 1 | ||||||||
| nstd187 | nssv16214977 | copy number variation | Sequencing | Read depth | No | HG02398 | GRCh38.p12 | NC_000008.11 | 8 | 7015373 | 7018816 | Remapped | 1 | ||||||||
| nstd187 | nssv16214978 | copy number variation | Sequencing | Read depth | No | HG00096 | GRCh38.p12 | NC_000008.11 | 8 | 7015373 | 7018816 | Remapped | 1 | ||||||||
| nstd187 | nssv16214979 | copy number variation | qPCR | Probe signal intensity | No | NA19129 | GRCh38.p12 | NC_000008.11 | 8 | 7015373 | 7018816 | Remapped | 1 | ||||||||
| nstd187 | nssv16214980 | copy number variation | qPCR | Probe signal intensity | No | NA19320 | GRCh38.p12 | NC_000008.11 | 8 | 7015373 | 7018816 | Remapped | 1 | ||||||||
| nstd187 | nssv16214981 | copy number variation | qPCR | Probe signal intensity | No | HG01890 | GRCh38.p12 | NC_000008.11 | 8 | 7015373 | 7018816 | Remapped | 1 | ||||||||
| nstd187 | nssv16214982 | copy number variation | qPCR | Probe signal intensity | No | HG02048 | GRCh38.p12 | NC_000008.11 | 8 | 7015373 | 7018816 | Remapped | 1 | ||||||||
| nstd187 | nssv16214983 | copy number variation | qPCR | Probe signal intensity | No | HG02360 | GRCh38.p12 | NC_000008.11 | 8 | 7015373 | 7018816 | Remapped | 1 | ||||||||
| nstd187 | nssv16214984 | copy number variation | qPCR | Probe signal intensity | No | NA18533 | GRCh38.p12 | NC_000008.11 | 8 | 7015373 | 7018816 | Remapped | 1 | ||||||||
| nstd187 | nssv16214985 | copy number variation | qPCR | Probe signal intensity | No | HG02067 | GRCh38.p12 | NC_000008.11 | 8 | 7015373 | 7018816 | Remapped | 1 | ||||||||
| nstd187 | nssv16214986 | copy number variation | qPCR | Probe signal intensity | No | HG02391 | GRCh38.p12 | NC_000008.11 | 8 | 7015373 | 7018816 | Remapped | 1 | ||||||||
| nstd187 | nssv16214987 | copy number variation | qPCR | Probe signal intensity | No | NA18870 | GRCh38.p12 | NC_000008.11 | 8 | 7015373 | 7018816 | Remapped | 1 | ||||||||
| nstd187 | nssv16214988 | copy number variation | qPCR | Probe signal intensity | No | HG03123 | GRCh38.p12 | NC_000008.11 | 8 | 7015373 | 7018816 | Remapped | 1 | ||||||||
| nstd187 | nssv16214989 | copy number variation | qPCR | Probe signal intensity | No | HG02554 | GRCh38.p12 | NC_000008.11 | 8 | 7015373 | 7018816 | Remapped | 1 | ||||||||
| nstd187 | nssv16214990 | copy number variation | Sequencing | Read depth | No | HG00978 | GRCh38.p12 | NC_000008.11 | 8 | 7015373 | 7018816 | Remapped | 1 | ||||||||
| nstd187 | nssv16214991 | copy number variation | Sequencing | Read depth | No | HG04002 | GRCh38.p12 | NC_000008.11 | 8 | 7015373 | 7018816 | Remapped | 1 | ||||||||
| nstd187 | nssv16214992 | copy number variation | Sequencing | Read depth | No | HG03103 | GRCh38.p12 | NC_000008.11 | 8 | 7015373 | 7018816 | Remapped | 1 | ||||||||
| nstd187 | nssv16214993 | copy number variation | Sequencing | Read depth | No | NA19437 | GRCh38.p12 | NC_000008.11 | 8 | 7015373 | 7018816 | Remapped | 1 | ||||||||
| nstd187 | nssv16214994 | copy number variation | Sequencing | Read depth | No | NA19222 | GRCh38.p12 | NC_000008.11 | 8 | 7015373 | 7018816 | Remapped | 1 | ||||||||
| nstd187 | nssv16214995 | copy number variation | Sequencing | Read depth | No | NA19076 | GRCh38.p12 | NC_000008.11 | 8 | 7015373 | 7018816 | Remapped | 1 | ||||||||
| nstd187 | nssv16214996 | copy number variation | Sequencing | Read depth | No | HG00143 | GRCh38.p12 | NC_000008.11 | 8 | 7015373 | 7018816 | Remapped | 1 | ||||||||
| nstd187 | nssv16214997 | copy number variation | Sequencing | Read depth | No | NA19711 | GRCh38.p12 | NC_000008.11 | 8 | 7015373 | 7018816 | Remapped | 1 | ||||||||
| nstd187 | nssv16214998 | copy number variation | Sequencing | Read depth | No | NA19658 | GRCh38.p12 | NC_000008.11 | 8 | 7015373 | 7018816 | Remapped | 1 | ||||||||
| nstd187 | nssv16214999 | copy number variation | Sequencing | Read depth | No | NA19679 | GRCh38.p12 | NC_000008.11 | 8 | 7015373 | 7018816 | Remapped | 1 | ||||||||
| nstd187 | nssv16215000 | copy number variation | Sequencing | Read depth | No | NA19722 | GRCh38.p12 | NC_000008.11 | 8 | 7015373 | 7018816 | Remapped | 1 | ||||||||
| nstd187 | nssv16215001 | copy number variation | Sequencing | Read depth | No | NA20346 | GRCh38.p12 | NC_000008.11 | 8 | 7015373 | 7018816 | Remapped | 1 | ||||||||
| nstd187 | nssv16215002 | copy number variation | Sequencing | Read depth | No | NA20362 | GRCh38.p12 | NC_000008.11 | 8 | 7015373 | 7018816 | Remapped | 1 | ||||||||
| nstd187 | nssv16215003 | copy number variation | Sequencing | Read depth | No | NA20508 | GRCh38.p12 | NC_000008.11 | 8 | 7015373 | 7018816 | Remapped | 1 | ||||||||
| nstd187 | nssv16215004 | copy number variation | Sequencing | Read depth | No | NA20502 | GRCh38.p12 | NC_000008.11 | 8 | 7015373 | 7018816 | Remapped | 1 | ||||||||
| nstd187 | nssv16215005 | copy number variation | Sequencing | Read depth | No | NA20355 | GRCh38.p12 | NC_000008.11 | 8 | 7015373 | 7018816 | Remapped | 1 | ||||||||
| nstd187 | nssv16215006 | copy number variation | Sequencing | Read depth | No | NA20356 | GRCh38.p12 | NC_000008.11 | 8 | 7015373 | 7018816 | Remapped | 1 | ||||||||
| nstd187 | nssv16215007 | copy number variation | Sequencing | Read depth | No | NA20340 | GRCh38.p12 | NC_000008.11 | 8 | 7015373 | 7018816 | Remapped | 1 | ||||||||
| nstd187 | nssv16215008 | copy number variation | Sequencing | Read depth | No | NA20348 | GRCh38.p12 | NC_000008.11 | 8 | 7015373 | 7018816 | Remapped | 1 | ||||||||
| nstd187 | nssv16215009 | copy number variation | Sequencing | Read depth | No | NA20274 | GRCh38.p12 | NC_000008.11 | 8 | 7015373 | 7018816 | Remapped | 1 | ||||||||
| nstd187 | nssv16215010 | copy number variation | Sequencing | Read depth | No | NA20126 | GRCh38.p12 | NC_000008.11 | 8 | 7015373 | 7018816 | Remapped | 1 | ||||||||
| nstd187 | nssv16215011 | copy number variation | Sequencing | Read depth | No | NA19921 | GRCh38.p12 | NC_000008.11 | 8 | 7015373 | 7018816 | Remapped | 1 | ||||||||
| nstd187 | nssv16215012 | copy number variation | Sequencing | Read depth | No | NA20287 | GRCh38.p12 | NC_000008.11 | 8 | 7015373 | 7018816 | Remapped | 1 | ||||||||
| nstd187 | nssv16215013 | copy number variation | Sequencing | Read depth | No | NA18878 | GRCh38.p12 | NC_000008.11 | 8 | 7015373 | 7018816 | Remapped | 1 | ||||||||
| nstd187 | nssv16215014 | copy number variation | Sequencing | Read depth | No | NA20334 | GRCh38.p12 | NC_000008.11 | 8 | 7015373 | 7018816 | Remapped | 1 | ||||||||
| nstd187 | nssv16215015 | copy number variation | Sequencing | Read depth | No | NA18954 | GRCh38.p12 | NC_000008.11 | 8 | 7015373 | 7018816 | Remapped | 1 | ||||||||
| nstd187 | nssv16215016 | copy number variation | Sequencing | Read depth | No | HG02624 | GRCh38.p12 | NC_000008.11 | 8 | 7015373 | 7018816 | Remapped | 1 | ||||||||
| nstd187 | nssv16215017 | copy number variation | Sequencing | Read depth | No | NA19376 | GRCh38.p12 | NC_000008.11 | 8 | 7015373 | 7018816 | Remapped | 1 | ||||||||
| nstd187 | nssv16215018 | copy number variation | Sequencing | Read depth | No | HG02798 | GRCh38.p12 | NC_000008.11 | 8 | 7015373 | 7018816 | Remapped | 1 | ||||||||
| nstd187 | nssv16215019 | copy number variation | Sequencing | Read depth | No | HG03246 | GRCh38.p12 | NC_000008.11 | 8 | 7015373 | 7018816 | Remapped | 1 | ||||||||
| nstd187 | nssv16215020 | copy number variation | Sequencing | Read depth | No | NA18968 | GRCh38.p12 | NC_000008.11 | 8 | 7015373 | 7018816 | Remapped | 1 | ||||||||
| nstd187 | nssv16215021 | copy number variation | Sequencing | Read depth | No | NA19129 | GRCh38.p12 | NC_000008.11 | 8 | 7015373 | 7018816 | Remapped | 1 | ||||||||
| nstd187 | nssv16215022 | copy number variation | Sequencing | Read depth | No | NA19320 | GRCh38.p12 | NC_000008.11 | 8 | 7015373 | 7018816 | Remapped | 1 | ||||||||
| nstd187 | nssv16215023 | copy number variation | Sequencing | Read depth | No | HG01890 | GRCh38.p12 | NC_000008.11 | 8 | 7015373 | 7018816 | Remapped | 1 | ||||||||
| nstd187 | nssv16215024 | copy number variation | Sequencing | Read depth | No | HG02048 | GRCh38.p12 | NC_000008.11 | 8 | 7015373 | 7018816 | Remapped | 1 | ||||||||
| nstd187 | nssv16215025 | copy number variation | Sequencing | Read depth | No | HG02360 | GRCh38.p12 | NC_000008.11 | 8 | 7015373 | 7018816 | Remapped | 1 | ||||||||
| nstd187 | nssv16215026 | copy number variation | Sequencing | Read depth | No | NA18533 | GRCh38.p12 | NC_000008.11 | 8 | 7015373 | 7018816 | Remapped | 1 | ||||||||
| nstd187 | nssv16215027 | copy number variation | Sequencing | Read depth | No | HG02067 | GRCh38.p12 | NC_000008.11 | 8 | 7015373 | 7018816 | Remapped | 1 | ||||||||
| nstd187 | nssv16215028 | copy number variation | Sequencing | Read depth | No | HG02391 | GRCh38.p12 | NC_000008.11 | 8 | 7015373 | 7018816 | Remapped | 1 | ||||||||
| nstd187 | nssv16215029 | copy number variation | Sequencing | Read depth | No | NA18870 | GRCh38.p12 | NC_000008.11 | 8 | 7015373 | 7018816 | Remapped | 1 | ||||||||
| nstd187 | nssv16215030 | copy number variation | Sequencing | Read depth | No | HG03123 | GRCh38.p12 | NC_000008.11 | 8 | 7015373 | 7018816 | Remapped | 1 | ||||||||
| nstd187 | nssv16215031 | copy number variation | Sequencing | Read depth | No | HG02554 | GRCh38.p12 | NC_000008.11 | 8 | 7015373 | 7018816 | Remapped | 1 | ||||||||
| nstd187 | nsv4684017 | copy number variation | No | GRCh38.p12 | NC_000008.11 | 8 | 7015373 | 7018816 | Remapped | 1 |