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nsv6795437

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:607

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 94 SVs from 20 studies. See in: genome view    
    Submitted genomic30,307,918-30,308,524Question Mark
    Overlapping variant regions from other studies: 94 SVs from 20 studies. See in: genome view    
    Remapped(Score: Perfect):30,275,695-30,276,301Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6795437Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000006.12Chr630,307,91830,308,524
    nsv6795437RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000006.11Chr630,275,69530,276,301

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18711275duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18711275Submitted genomicNC_000006.12:g.303
    07918_30308524dup
    GRCh38 (hg38)NC_000006.12Chr630,307,91830,308,524
    nssv18711275RemappedPerfectNC_000006.11:g.302
    75695_30276301dup
    GRCh37.p13First PassNC_000006.11Chr630,275,69530,276,301

    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)
    nssv187112758e-062245482
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