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nsv6896392

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:7,554

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 104 SVs from 32 studies. See in: genome view    
    Submitted genomic14,605,409-14,612,962Question Mark
    Overlapping variant regions from other studies: 104 SVs from 32 studies. See in: genome view    
    Remapped(Score: Perfect):14,647,408-14,654,961Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6896392Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000010.11Chr1014,605,40914,612,962
    nsv6896392RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000010.10Chr1014,647,40814,654,961

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18333797deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18333797Submitted genomicNC_000010.11:g.146
    05409_14612962del
    GRCh38 (hg38)NC_000010.11Chr1014,605,40914,612,962
    nssv18333797RemappedPerfectNC_000010.10:g.146
    47408_14654961del
    GRCh37.p13First PassNC_000010.10Chr1014,647,40814,654,961

    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)
    nssv183337977e-062276070
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