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nsv6998324

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:7,892

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 153 SVs from 38 studies. See in: genome view    
    Submitted genomic56,186,417-56,194,308Question Mark
    Overlapping variant regions from other studies: 153 SVs from 38 studies. See in: genome view    
    Remapped(Score: Perfect):56,697,786-56,705,677Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6998324Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000019.10Chr1956,186,41756,194,308
    nsv6998324RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000019.9Chr1956,697,78656,705,677

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18639019duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18639019Submitted genomicNC_000019.10:g.561
    86417_56194308dup
    GRCh38 (hg38)NC_000019.10Chr1956,186,41756,194,308
    nssv18639019RemappedPerfectNC_000019.9:g.5669
    7786_56705677dup
    GRCh37.p13First PassNC_000019.9Chr1956,697,78656,705,677

    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)
    nssv186390194e-061275908
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