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nsv6824671

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:7,324

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 118 SVs from 37 studies. See in: genome view    
    Submitted genomic55,955,935-55,963,258Question Mark
    Overlapping variant regions from other studies: 118 SVs from 37 studies. See in: genome view    
    Remapped(Score: Perfect):56,023,628-56,030,951Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6824671Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000007.14Chr755,955,93555,963,258
    nsv6824671RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000007.13Chr756,023,62856,030,951

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18546831deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18546831Submitted genomicNC_000007.14:g.559
    55935_55963258del
    GRCh38 (hg38)NC_000007.14Chr755,955,93555,963,258
    nssv18546831RemappedPerfectNC_000007.13:g.560
    23628_56030951del
    GRCh37.p13First PassNC_000007.13Chr756,023,62856,030,951

    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)
    nssv185468314e-061276162
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