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nsv6912929

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:13,468

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 132 SVs from 41 studies. See in: genome view    
    Submitted genomic3,377,304-3,390,771Question Mark
    Overlapping variant regions from other studies: 132 SVs from 41 studies. See in: genome view    
    Remapped(Score: Perfect):3,398,534-3,412,001Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6912929Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000011.10Chr113,377,3043,390,771
    nsv6912929RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000011.9Chr113,398,5343,412,001

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18349053deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18349053Submitted genomicNC_000011.10:g.337
    7304_3390771del
    GRCh38 (hg38)NC_000011.10Chr113,377,3043,390,771
    nssv18349053RemappedPerfectNC_000011.9:g.3398
    534_3412001del
    GRCh37.p13First PassNC_000011.9Chr113,398,5343,412,001

    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)
    nssv183490537e-062276190
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