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nsv6400401

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:11,100

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 143 SVs from 27 studies. See in: genome view    
    Submitted genomic115,835,301-115,846,400Question Mark
    Overlapping variant regions from other studies: 143 SVs from 27 studies. See in: genome view    
    Remapped(Score: Perfect):115,170,998-115,182,097Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6400401Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000005.10Chr5115,835,301115,846,400
    nsv6400401RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000005.9Chr5115,170,998115,182,097

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18212469duplicationSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18212469Submitted genomicNC_000005.10:g.115
    835301_115846400du
    p
    GRCh38 (hg38)NC_000005.10Chr5115,835,301115,846,400
    nssv18212469RemappedPerfectNC_000005.9:g.1151
    70998_115182097dup
    GRCh37.p13First PassNC_000005.9Chr5115,170,998115,182,097

    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)
    nssv18212469<0.001439238
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