U.S. flag

An official website of the United States government

nsv7074171

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,857,431

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 4930 SVs from 113 studies. See in: genome view    
    Submitted genomic27,576,188-29,433,618Question Mark
    Overlapping variant regions from other studies: 4970 SVs from 113 studies. See in: genome view    
    Remapped(Score: Good):27,821,334-29,725,822Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7074171Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000015.10Chr1527,576,18829,433,618
    nsv7074171RemappedGoodGRCh37.p13Primary AssemblyFirst PassNC_000015.9Chr1527,821,33429,725,822

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18755961inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18755961Submitted genomicNC_000015.10:g.275
    76188_29433618inv
    GRCh38 (hg38)NC_000015.10Chr1527,576,18829,433,618
    nssv18755961RemappedGoodNC_000015.9:g.2782
    1334_29725822inv
    GRCh37.p13First PassNC_000015.9Chr1527,821,33429,725,822

    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)
    nssv187559611.1e-053274738
    Support Center