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nsv6952982

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:5,822

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 60 SVs from 20 studies. See in: genome view    
    Submitted genomic24,378,921-24,384,742Question Mark
    Overlapping variant regions from other studies: 61 SVs from 21 studies. See in: genome view    
    Remapped(Score: Perfect):24,848,127-24,853,948Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6952982Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000014.9Chr1424,378,92124,384,742
    nsv6952982RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000014.8Chr1424,848,12724,853,948

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18384892deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18384892Submitted genomicNC_000014.9:g.2437
    8921_24384742del
    GRCh38 (hg38)NC_000014.9Chr1424,378,92124,384,742
    nssv18384892RemappedPerfectNC_000014.8:g.2484
    8127_24853948del
    GRCh37.p13First PassNC_000014.8Chr1424,848,12724,853,948

    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)
    nssv183848921.4e-054276208
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