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nsv7020179

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:105

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 252 SVs from 20 studies. See in: genome view    
    Submitted genomic40,711,504-40,711,608Question Mark
    Overlapping variant regions from other studies: 252 SVs from 20 studies. See in: genome view    
    Remapped(Score: Perfect):40,570,756-40,570,860Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7020179Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000023.11ChrX40,711,50440,711,608
    nsv7020179RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000023.10ChrX40,570,75640,570,860

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18766234inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18766234Submitted genomicNC_000023.11:g.407
    11504_40711608inv
    GRCh38 (hg38)NC_000023.11ChrX40,711,50440,711,608
    nssv18766234RemappedPerfectNC_000023.10:g.405
    70756_40570860inv
    GRCh37.p13First PassNC_000023.10ChrX40,570,75640,570,860

    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)
    nssv187662340.001247216667
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