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nsv6764672

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:2,780

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 103 SVs from 24 studies. See in: genome view    
    Submitted genomic31,274,267-31,277,046Question Mark
    Overlapping variant regions from other studies: 103 SVs from 24 studies. See in: genome view    
    Remapped(Score: Perfect):31,274,374-31,277,153Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6764672Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000005.10Chr531,274,26731,277,046
    nsv6764672RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000005.9Chr531,274,37431,277,153

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18513953deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18513953Submitted genomicNC_000005.10:g.312
    74267_31277046del
    GRCh38 (hg38)NC_000005.10Chr531,274,26731,277,046
    nssv18513953RemappedPerfectNC_000005.9:g.3127
    4374_31277153del
    GRCh37.p13First PassNC_000005.9Chr531,274,37431,277,153

    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)
    nssv185139533.2e-059275674
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