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nsv6726183

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:10,358

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 123 SVs from 23 studies. See in: genome view    
    Submitted genomic154,427,590-154,437,947Question Mark
    Overlapping variant regions from other studies: 123 SVs from 23 studies. See in: genome view    
    Remapped(Score: Perfect):154,145,379-154,155,736Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6726183Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000003.12Chr3154,427,590154,437,947
    nsv6726183RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000003.11Chr3154,145,379154,155,736

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18671829duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18671829Submitted genomicNC_000003.12:g.154
    427590_154437947du
    p
    GRCh38 (hg38)NC_000003.12Chr3154,427,590154,437,947
    nssv18671829RemappedPerfectNC_000003.11:g.154
    145379_154155736du
    p
    GRCh37.p13First PassNC_000003.11Chr3154,145,379154,155,736

    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)
    nssv186718294e-061275692
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