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nsv6640484

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:70,700

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 206 SVs from 32 studies. See in: genome view    
    Submitted genomic116,933,801-117,004,500Question Mark
    Overlapping variant regions from other studies: 208 SVs from 32 studies. See in: genome view    
    Remapped(Score: Perfect):117,476,423-117,547,122Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6640484Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr1116,933,801117,004,500
    nsv6640484RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr1117,476,423117,547,122

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18581074duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18581074Submitted genomicNC_000001.11:g.116
    933801_117004500du
    p
    GRCh38 (hg38)NC_000001.11Chr1116,933,801117,004,500
    nssv18581074RemappedPerfectNC_000001.10:g.117
    476423_117547122du
    p
    GRCh37.p13First PassNC_000001.10Chr1117,476,423117,547,122

    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)
    nssv185810741.4e-054270092
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