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nsv7063220

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,263,456

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 3439 SVs from 89 studies. See in: genome view    
    Submitted genomic55,051,178-56,314,633Question Mark
    Overlapping variant regions from other studies: 3439 SVs from 89 studies. See in: genome view    
    Remapped(Score: Perfect):55,343,376-56,606,831Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7063220Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000015.10Chr1555,051,17856,314,633
    nsv7063220RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000015.9Chr1555,343,37656,606,831

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18756282inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18756282Submitted genomicNC_000015.10:g.550
    51178_56314633inv
    GRCh38 (hg38)NC_000015.10Chr1555,051,17856,314,633
    nssv18756282RemappedPerfectNC_000015.9:g.5534
    3376_56606831inv
    GRCh37.p13First PassNC_000015.9Chr1555,343,37656,606,831

    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)
    nssv187562824e-061276268
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