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nsv6914790

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:4,132

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 172 SVs from 45 studies. See in: genome view    
    Submitted genomic4,568,229-4,572,360Question Mark
    Overlapping variant regions from other studies: 172 SVs from 45 studies. See in: genome view    
    Remapped(Score: Perfect):4,589,459-4,593,590Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6914790Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000011.10Chr114,568,2294,572,360
    nsv6914790RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000011.9Chr114,589,4594,593,590

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18350071deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18350071Submitted genomicNC_000011.10:g.456
    8229_4572360del
    GRCh38 (hg38)NC_000011.10Chr114,568,2294,572,360
    nssv18350071RemappedPerfectNC_000011.9:g.4589
    459_4593590del
    GRCh37.p13First PassNC_000011.9Chr114,589,4594,593,590

    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)
    nssv183500714e-060275782
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