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nsv6969791

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:139,940

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 738 SVs from 76 studies. See in: genome view    
    Submitted genomic2,939,852-3,079,791Question Mark
    Overlapping variant regions from other studies: 738 SVs from 76 studies. See in: genome view    
    Remapped(Score: Perfect):2,989,853-3,129,792Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6969791Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000016.10Chr162,939,8523,079,791
    nsv6969791RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000016.9Chr162,989,8533,129,792

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18400893deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18400893Submitted genomicNC_000016.10:g.293
    9852_3079791del
    GRCh38 (hg38)NC_000016.10Chr162,939,8523,079,791
    nssv18400893RemappedPerfectNC_000016.9:g.2989
    853_3129792del
    GRCh37.p13First PassNC_000016.9Chr162,989,8533,129,792

    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)
    nssv184008937e-062276184
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