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nsv6821443

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:392

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 135 SVs from 31 studies. See in: genome view    
    Submitted genomic140,415,727-140,416,118Question Mark
    Overlapping variant regions from other studies: 135 SVs from 31 studies. See in: genome view    
    Remapped(Score: Perfect):140,115,527-140,115,918Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6821443Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000007.14Chr7140,415,727140,416,118
    nsv6821443RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000007.13Chr7140,115,527140,115,918

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18535796deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18535796Submitted genomicNC_000007.14:g.140
    415727_140416118de
    l
    GRCh38 (hg38)NC_000007.14Chr7140,415,727140,416,118
    nssv18535796RemappedPerfectNC_000007.13:g.140
    115527_140115918de
    l
    GRCh37.p13First PassNC_000007.13Chr7140,115,527140,115,918

    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)
    nssv18535796<0.001253256512
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