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nsv7055271

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:5,657,757

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 9336 SVs from 89 studies. See in: genome view    
    Submitted genomic114,091,775-119,749,531Question Mark
    Overlapping variant regions from other studies: 5677 SVs from 81 studies. See in: genome view    
    Remapped(Score: Pass):115,732,291-118,883,494Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7055271Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000023.11ChrX114,091,775119,749,531
    nsv7055271RemappedPassGRCh37.p13Primary AssemblyFirst PassNC_000023.10ChrX115,732,291118,883,494

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18763933inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18763933Submitted genomicNC_000023.11:g.114
    091775_119749531in
    v
    GRCh38 (hg38)NC_000023.11ChrX114,091,775119,749,531
    nssv18763933RemappedPassNC_000023.10:g.115
    732291_118883494in
    v
    GRCh37.p13First PassNC_000023.10ChrX115,732,291118,883,494

    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)
    nssv187639335e-061200000
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