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nsv7070354

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:50,015

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 272 SVs from 53 studies. See in: genome view    
    Submitted genomic86,461,729-86,511,743Question Mark
    Overlapping variant regions from other studies: 272 SVs from 53 studies. See in: genome view    
    Remapped(Score: Perfect):86,855,506-86,905,520Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7070354Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000012.12Chr1286,461,72986,511,743
    nsv7070354RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000012.11Chr1286,855,50686,905,520

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18753212inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18753212Submitted genomicNC_000012.12:g.864
    61729_86511743inv
    GRCh38 (hg38)NC_000012.12Chr1286,461,72986,511,743
    nssv18753212RemappedPerfectNC_000012.11:g.868
    55506_86905520inv
    GRCh37.p13First PassNC_000012.11Chr1286,855,50686,905,520

    No validation data were submitted for this variant

    No clinical assertion data were submitted for this variant

    Complete genotype and/or allele frequency data for this study can be found on dbVar's FTP site.

    Genotype Information

    Variant Call IDAllele Frequency (AF)Allele Count (AC)Allele Number (AN)
    nssv187532121.4e-054274864
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