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nsv6917869

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:62,900

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 625 SVs from 78 studies. See in: genome view    
    Submitted genomic49,639,101-49,702,000Question Mark
    Overlapping variant regions from other studies: 625 SVs from 78 studies. See in: genome view    
    Remapped(Score: Perfect):49,660,653-49,723,552Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6917869Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000011.10Chr1149,639,10149,702,000
    nsv6917869RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000011.9Chr1149,660,65349,723,552

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18350482deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18350482Submitted genomicNC_000011.10:g.496
    39101_49702000del
    GRCh38 (hg38)NC_000011.10Chr1149,639,10149,702,000
    nssv18350482RemappedPerfectNC_000011.9:g.4966
    0653_49723552del
    GRCh37.p13First PassNC_000011.9Chr1149,660,65349,723,552

    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)
    nssv18350482<0.00128238738
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