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nsv6912403

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:161,143

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 558 SVs from 71 studies. See in: genome view    
    Submitted genomic6,840,585-7,001,727Question Mark
    Overlapping variant regions from other studies: 558 SVs from 71 studies. See in: genome view    
    Remapped(Score: Perfect):6,861,816-7,022,958Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6912403Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000011.10Chr116,840,5857,001,727
    nsv6912403RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000011.9Chr116,861,8167,022,958

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18351375deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18351375Submitted genomicNC_000011.10:g.684
    0585_7001727del
    GRCh38 (hg38)NC_000011.10Chr116,840,5857,001,727
    nssv18351375RemappedPerfectNC_000011.9:g.6861
    816_7022958del
    GRCh37.p13First PassNC_000011.9Chr116,861,8167,022,958

    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)
    nssv183513754e-061276182
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