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nsv6748250

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:2,998,372

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 8946 SVs from 109 studies. See in: genome view    
    Submitted genomic179,729,233-182,727,604Question Mark
    Overlapping variant regions from other studies: 8946 SVs from 109 studies. See in: genome view    
    Remapped(Score: Perfect):180,650,386-183,648,757Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6748250Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000004.12Chr4179,729,233182,727,604
    nsv6748250RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000004.11Chr4180,650,386183,648,757

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18491621deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18491621Submitted genomicNC_000004.12:g.179
    729233_182727604de
    l
    GRCh38 (hg38)NC_000004.12Chr4179,729,233182,727,604
    nssv18491621RemappedPerfectNC_000004.11:g.180
    650386_183648757de
    l
    GRCh37.p13First PassNC_000004.11Chr4180,650,386183,648,757

    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)
    nssv184916214e-061276156
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