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nsv6995201

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:3,317

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 85 SVs from 17 studies. See in: genome view    
    Submitted genomic27,983,071-27,986,387Question Mark
    Overlapping variant regions from other studies: 85 SVs from 17 studies. See in: genome view    
    Remapped(Score: Perfect):27,994,392-27,997,708Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6995201Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000016.10Chr1627,983,07127,986,387
    nsv6995201RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000016.9Chr1627,994,39227,997,708

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18622234duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18622234Submitted genomicNC_000016.10:g.279
    83071_27986387dup
    GRCh38 (hg38)NC_000016.10Chr1627,983,07127,986,387
    nssv18622234RemappedPerfectNC_000016.9:g.2799
    4392_27997708dup
    GRCh37.p13First PassNC_000016.9Chr1627,994,39227,997,708

    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)
    nssv186222343.2e-059273970
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