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nsv6405985

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,200

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 133 SVs from 23 studies. See in: genome view    
    Submitted genomic115,873,801-115,875,000Question Mark
    Overlapping variant regions from other studies: 133 SVs from 23 studies. See in: genome view    
    Remapped(Score: Perfect):115,209,498-115,210,697Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6405985Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000005.10Chr5115,873,801115,875,000
    nsv6405985RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000005.9Chr5115,209,498115,210,697

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18125651deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18125651Submitted genomicNC_000005.10:g.115
    873801_115875000de
    l
    GRCh38 (hg38)NC_000005.10Chr5115,873,801115,875,000
    nssv18125651RemappedPerfectNC_000005.9:g.1152
    09498_115210697del
    GRCh37.p13First PassNC_000005.9Chr5115,209,498115,210,697

    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)
    nssv18125651<0.0011138570
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