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nsv7053078

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:62

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 244 SVs from 17 studies. See in: genome view    
    Submitted genomic108,107,330-108,107,391Question Mark
    Overlapping variant regions from other studies: 244 SVs from 17 studies. See in: genome view    
    Remapped(Score: Perfect):107,350,560-107,350,621Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7053078Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000023.11ChrX108,107,330108,107,391
    nsv7053078RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000023.10ChrX107,350,560107,350,621

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18765666inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18765666Submitted genomicNC_000023.11:g.108
    107330_108107391in
    v
    GRCh38 (hg38)NC_000023.11ChrX108,107,330108,107,391
    nssv18765666RemappedPerfectNC_000023.10:g.107
    350560_107350621in
    v
    GRCh37.p13First PassNC_000023.10ChrX107,350,560107,350,621

    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)
    nssv187656665e-061200000
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