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nsv7064571

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:42,657

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 330 SVs from 62 studies. See in: genome view    
    Submitted genomic38,296,904-38,339,560Question Mark
    Overlapping variant regions from other studies: 330 SVs from 62 studies. See in: genome view    
    Remapped(Score: Perfect):38,690,706-38,733,362Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7064571Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000012.12Chr1238,296,90438,339,560
    nsv7064571RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000012.11Chr1238,690,70638,733,362

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18752663inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18752663Submitted genomicNC_000012.12:g.382
    96904_38339560inv
    GRCh38 (hg38)NC_000012.12Chr1238,296,90438,339,560
    nssv18752663RemappedPerfectNC_000012.11:g.386
    90706_38733362inv
    GRCh37.p13First PassNC_000012.11Chr1238,690,70638,733,362

    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)
    nssv187526634e-061276268
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