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nsv6949862

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:5,872,774

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 13744 SVs from 106 studies. See in: genome view    
    Submitted genomic51,123,112-56,995,885Question Mark
    Overlapping variant regions from other studies: 13743 SVs from 106 studies. See in: genome view    
    Remapped(Score: Perfect):51,589,830-57,462,603Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6949862Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000014.9Chr1451,123,11256,995,885
    nsv6949862RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000014.8Chr1451,589,83057,462,603

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18386956deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18386956Submitted genomicNC_000014.9:g.5112
    3112_56995885del
    GRCh38 (hg38)NC_000014.9Chr1451,123,11256,995,885
    nssv18386956RemappedPerfectNC_000014.8:g.5158
    9830_57462603del
    GRCh37.p13First PassNC_000014.8Chr1451,589,83057,462,603

    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)
    nssv183869564e-061276160
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