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nsv7056095

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:945,693

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 2322 SVs from 90 studies. See in: genome view    
    Submitted genomic52,719,057-53,664,749Question Mark
    Overlapping variant regions from other studies: 2322 SVs from 90 studies. See in: genome view    
    Remapped(Score: Perfect):52,014,891-52,960,579Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7056095Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000005.10Chr552,719,05753,664,749
    nsv7056095RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000005.9Chr552,014,89152,960,579

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18776927inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18776927Submitted genomicNC_000005.10:g.527
    19057_53664749inv
    GRCh38 (hg38)NC_000005.10Chr552,719,05753,664,749
    nssv18776927RemappedPerfectNC_000005.9:g.5201
    4891_52960579inv
    GRCh37.p13First PassNC_000005.9Chr552,014,89152,960,579

    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)
    nssv187769274e-061276268
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