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nsv7063669

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:4,271

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 159 SVs from 48 studies. See in: genome view    
    Submitted genomic37,937,897-37,942,167Question Mark
    Overlapping variant regions from other studies: 159 SVs from 48 studies. See in: genome view    
    Remapped(Score: Perfect):37,959,447-37,963,717Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7063669Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000011.10Chr1137,937,89737,942,167
    nsv7063669RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000011.9Chr1137,959,44737,963,717

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18746122inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18746122Submitted genomicNC_000011.10:g.379
    37897_37942167inv
    GRCh38 (hg38)NC_000011.10Chr1137,937,89737,942,167
    nssv18746122RemappedPerfectNC_000011.9:g.3795
    9447_37963717inv
    GRCh37.p13First PassNC_000011.9Chr1137,959,44737,963,717

    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)
    nssv187461224e-061276268
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