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nsv7057597

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:587,983

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 1864 SVs from 76 studies. See in: genome view    
    Submitted genomic40,706,162-41,294,144Question Mark
    Overlapping variant regions from other studies: 1864 SVs from 76 studies. See in: genome view    
    Remapped(Score: Perfect):40,708,179-41,296,161Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7057597Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000004.12Chr440,706,16241,294,144
    nsv7057597RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000004.11Chr440,708,17941,296,161

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18774184inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18774184Submitted genomicNC_000004.12:g.407
    06162_41294144inv
    GRCh38 (hg38)NC_000004.12Chr440,706,16241,294,144
    nssv18774184RemappedPerfectNC_000004.11:g.407
    08179_41296161inv
    GRCh37.p13First PassNC_000004.11Chr440,708,17941,296,161

    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)
    nssv187741844e-061276268
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