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nsv6908779

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:6,457

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 104 SVs from 29 studies. See in: genome view    
    Submitted genomic66,930,360-66,936,816Question Mark
    Overlapping variant regions from other studies: 104 SVs from 29 studies. See in: genome view    
    Remapped(Score: Perfect):66,697,831-66,704,287Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6908779Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000011.10Chr1166,930,36066,936,816
    nsv6908779RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000011.9Chr1166,697,83166,704,287

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18579660duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18579660Submitted genomicNC_000011.10:g.669
    30360_66936816dup
    GRCh38 (hg38)NC_000011.10Chr1166,930,36066,936,816
    nssv18579660RemappedPerfectNC_000011.9:g.6669
    7831_66704287dup
    GRCh37.p13First PassNC_000011.9Chr1166,697,83166,704,287

    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)
    nssv185796604e-061275734
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