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nsv7027510

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:20,782

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 252 SVs from 30 studies. See in: genome view    
    Submitted genomic68,678,051-68,698,832Question Mark
    Overlapping variant regions from other studies: 252 SVs from 30 studies. See in: genome view    
    Remapped(Score: Perfect):67,897,893-67,918,674Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7027510Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000023.11ChrX68,678,05168,698,832
    nsv7027510RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000023.10ChrX67,897,89367,918,674

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18767125inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18767125Submitted genomicNC_000023.11:g.686
    78051_68698832inv
    GRCh38 (hg38)NC_000023.11ChrX68,678,05168,698,832
    nssv18767125RemappedPerfectNC_000023.10:g.678
    97893_67918674inv
    GRCh37.p13First PassNC_000023.10ChrX67,897,89367,918,674

    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)
    nssv187671255e-061200000
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