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nsv6656681

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:10,199

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 127 SVs from 26 studies. See in: genome view    
    Submitted genomic94,295,121-94,305,319Question Mark
    Overlapping variant regions from other studies: 127 SVs from 26 studies. See in: genome view    
    Remapped(Score: Perfect):94,760,677-94,770,875Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6656681Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr194,295,12194,305,319
    nsv6656681RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr194,760,67794,770,875

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18428097deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18428097Submitted genomicNC_000001.11:g.942
    95121_94305319del
    GRCh38 (hg38)NC_000001.11Chr194,295,12194,305,319
    nssv18428097RemappedPerfectNC_000001.10:g.947
    60677_94770875del
    GRCh37.p13First PassNC_000001.10Chr194,760,67794,770,875

    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)
    nssv184280974e-061276172
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