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nsv6974463

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:4,485

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 891 SVs from 70 studies. See in: genome view    
    Submitted genomic22,962,562-22,967,046Question Mark
    Overlapping variant regions from other studies: 1113 SVs from 73 studies. See in: genome view    
    Remapped(Score: Perfect):22,906,022-22,910,506Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6974463Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000015.10Chr1522,962,56222,967,046
    nsv6974463RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000015.9Chr1522,906,02222,910,506

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18393282deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18393282Submitted genomicNC_000015.10:g.229
    62562_22967046del
    GRCh38 (hg38)NC_000015.10Chr1522,962,56222,967,046
    nssv18393282RemappedPerfectNC_000015.9:g.2290
    6022_22910506del
    GRCh37.p13First PassNC_000015.9Chr1522,906,02222,910,506

    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)
    nssv183932824e-061275610
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