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nsv6728150

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:5,400

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 134 SVs from 24 studies. See in: genome view    
    Submitted genomic150,865,901-150,871,300Question Mark
    Overlapping variant regions from other studies: 134 SVs from 24 studies. See in: genome view    
    Remapped(Score: Perfect):150,583,688-150,589,087Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6728150Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000003.12Chr3150,865,901150,871,300
    nsv6728150RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000003.11Chr3150,583,688150,589,087

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18474121deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18474121Submitted genomicNC_000003.12:g.150
    865901_150871300de
    l
    GRCh38 (hg38)NC_000003.12Chr3150,865,901150,871,300
    nssv18474121RemappedPerfectNC_000003.11:g.150
    583688_150589087de
    l
    GRCh37.p13First PassNC_000003.11Chr3150,583,688150,589,087

    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)
    nssv184741214e-061276174
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