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nsv7074060

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:159,147

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 641 SVs from 71 studies. See in: genome view    
    Submitted genomic51,672,076-51,831,222Question Mark
    Overlapping variant regions from other studies: 641 SVs from 71 studies. See in: genome view    
    Remapped(Score: Perfect):52,584,636-52,743,782Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7074060Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000008.11Chr851,672,07651,831,222
    nsv7074060RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000008.10Chr852,584,63652,743,782

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18782488inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18782488Submitted genomicNC_000008.11:g.516
    72076_51831222inv
    GRCh38 (hg38)NC_000008.11Chr851,672,07651,831,222
    nssv18782488RemappedPerfectNC_000008.10:g.525
    84636_52743782inv
    GRCh37.p13First PassNC_000008.10Chr852,584,63652,743,782

    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)
    nssv18782488<0.00143269846
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