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nsv6907486

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:146,951

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 559 SVs from 71 studies. See in: genome view    
    Submitted genomic6,769,718-6,916,668Question Mark
    Overlapping variant regions from other studies: 559 SVs from 71 studies. See in: genome view    
    Remapped(Score: Perfect):6,790,949-6,937,899Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6907486Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000011.10Chr116,769,7186,916,668
    nsv6907486RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000011.9Chr116,790,9496,937,899

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18353130deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18353130Submitted genomicNC_000011.10:g.676
    9718_6916668del
    GRCh38 (hg38)NC_000011.10Chr116,769,7186,916,668
    nssv18353130RemappedPerfectNC_000011.9:g.6790
    949_6937899del
    GRCh37.p13First PassNC_000011.9Chr116,790,9496,937,899

    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)
    nssv183531307e-062276152
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