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nsv6319875

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:410

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 112 SVs from 26 studies. See in: genome view    
    Submitted genomic31,694,292-31,694,701Question Mark
    Overlapping variant regions from other studies: 112 SVs from 26 studies. See in: genome view    
    Remapped(Score: Perfect):32,159,893-32,160,302Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6319875Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr131,694,29231,694,701
    nsv6319875RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr132,159,89332,160,302

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18060400deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18060400Submitted genomicNC_000001.11:g.316
    94292_31694701del
    GRCh38 (hg38)NC_000001.11Chr131,694,29231,694,701
    nssv18060400RemappedPerfectNC_000001.10:g.321
    59893_32160302del
    GRCh37.p13First PassNC_000001.10Chr132,159,89332,160,302

    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)
    nssv18060400<0.001134724
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