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nsv6452469

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:7,988

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 140 SVs from 26 studies. See in: genome view    
    Submitted genomic132,367,719-132,375,706Question Mark
    Overlapping variant regions from other studies: 140 SVs from 26 studies. See in: genome view    
    Remapped(Score: Perfect):135,243,106-135,251,093Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6452469Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000009.12Chr9132,367,719132,375,706
    nsv6452469RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000009.11Chr9135,243,106135,251,093

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18177043deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18177043Submitted genomicNC_000009.12:g.132
    367719_132375706de
    l
    GRCh38 (hg38)NC_000009.12Chr9132,367,719132,375,706
    nssv18177043RemappedPerfectNC_000009.11:g.135
    243106_135251093de
    l
    GRCh37.p13First PassNC_000009.11Chr9135,243,106135,251,093

    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)
    nssv18177043<0.001139290
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