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nsv6977331

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:3,700

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 138 SVs from 27 studies. See in: genome view    
    Submitted genomic3,963,001-3,966,700Question Mark
    Overlapping variant regions from other studies: 138 SVs from 27 studies. See in: genome view    
    Remapped(Score: Perfect):4,013,002-4,016,701Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6977331Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000016.10Chr163,963,0013,966,700
    nsv6977331RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000016.9Chr164,013,0024,016,701

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18400922deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18400922Submitted genomicNC_000016.10:g.396
    3001_3966700del
    GRCh38 (hg38)NC_000016.10Chr163,963,0013,966,700
    nssv18400922RemappedPerfectNC_000016.9:g.4013
    002_4016701del
    GRCh37.p13First PassNC_000016.9Chr164,013,0024,016,701

    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)
    nssv184009224e-061275774
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