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nsv7042863

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:265,409

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 918 SVs from 71 studies. See in: genome view    
    Submitted genomic85,463,758-85,729,166Question Mark
    Overlapping variant regions from other studies: 918 SVs from 71 studies. See in: genome view    
    Remapped(Score: Perfect):85,690,881-85,956,289Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7042863Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000002.12Chr285,463,75885,729,166
    nsv7042863RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000002.11Chr285,690,88185,956,289

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18769473inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18769473Submitted genomicNC_000002.12:g.854
    63758_85729166inv
    GRCh38 (hg38)NC_000002.12Chr285,463,75885,729,166
    nssv18769473RemappedPerfectNC_000002.11:g.856
    90881_85956289inv
    GRCh37.p13First PassNC_000002.11Chr285,690,88185,956,289

    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)
    nssv187694737e-062275938
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