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nsv6831006

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:60,400

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 368 SVs from 50 studies. See in: genome view    
    Submitted genomic47,747,301-47,807,700Question Mark
    Overlapping variant regions from other studies: 368 SVs from 50 studies. See in: genome view    
    Remapped(Score: Perfect):47,786,899-47,847,298Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6831006Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000007.14Chr747,747,30147,807,700
    nsv6831006RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000007.13Chr747,786,89947,847,298

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18543258deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18543258Submitted genomicNC_000007.14:g.477
    47301_47807700del
    GRCh38 (hg38)NC_000007.14Chr747,747,30147,807,700
    nssv18543258RemappedPerfectNC_000007.13:g.477
    86899_47847298del
    GRCh37.p13First PassNC_000007.13Chr747,786,89947,847,298

    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)
    nssv185432584e-061276172
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