U.S. flag

An official website of the United States government

nsv7064472

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:6,441,448

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 16163 SVs from 126 studies. See in: genome view    
    Submitted genomic73,034,378-79,475,825Question Mark
    Overlapping variant regions from other studies: 16165 SVs from 126 studies. See in: genome view    
    Remapped(Score: Perfect):73,326,719-79,768,167Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7064472Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000015.10Chr1573,034,37879,475,825
    nsv7064472RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000015.9Chr1573,326,71979,768,167

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18755055inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18755055Submitted genomicNC_000015.10:g.730
    34378_79475825inv
    GRCh38 (hg38)NC_000015.10Chr1573,034,37879,475,825
    nssv18755055RemappedPerfectNC_000015.9:g.7332
    6719_79768167inv
    GRCh37.p13First PassNC_000015.9Chr1573,326,71979,768,167

    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)
    nssv187550554e-061276268
    Support Center