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nsv6531500

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:590

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 172 SVs from 19 studies. See in: genome view    
    Submitted genomic31,134,114-31,134,703Question Mark
    Overlapping variant regions from other studies: 172 SVs from 19 studies. See in: genome view    
    Remapped(Score: Perfect):28,714,077-28,714,666Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6531500Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000018.10Chr1831,134,11431,134,703
    nsv6531500RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000018.9Chr1828,714,07728,714,666

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18039896deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18039896Submitted genomicNC_000018.10:g.311
    34114_31134703del
    GRCh38 (hg38)NC_000018.10Chr1831,134,11431,134,703
    nssv18039896RemappedPerfectNC_000018.9:g.2871
    4077_28714666del
    GRCh37.p13First PassNC_000018.9Chr1828,714,07728,714,666

    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)
    nssv18039896<0.001737744
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