U.S. flag

An official website of the United States government

nsv7065172

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:4,452

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 162 SVs from 19 studies. See in: genome view    
    Submitted genomic94,018,326-94,022,777Question Mark
    Overlapping variant regions from other studies: 162 SVs from 19 studies. See in: genome view    
    Remapped(Score: Perfect):94,670,580-94,675,031Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7065172Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000013.11Chr1394,018,32694,022,777
    nsv7065172RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000013.10Chr1394,670,58094,675,031

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18754890inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18754890Submitted genomicNC_000013.11:g.940
    18326_94022777inv
    GRCh38 (hg38)NC_000013.11Chr1394,018,32694,022,777
    nssv18754890RemappedPerfectNC_000013.10:g.946
    70580_94675031inv
    GRCh37.p13First PassNC_000013.10Chr1394,670,58094,675,031

    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)
    nssv187548907e-062276266
    Support Center