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nsv6348430

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:3,828,727

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 15077 SVs from 120 studies. See in: genome view    
    Submitted genomic237,953,314-241,782,040Question Mark
    Overlapping variant regions from other studies: 15015 SVs from 120 studies. See in: genome view    
    Remapped(Score: Good):238,861,956-242,721,455Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6348430Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000002.12Chr2237,953,314241,782,040
    nsv6348430RemappedGoodGRCh37.p13Primary AssemblyFirst PassNC_000002.11Chr2238,861,956242,721,455

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18208369duplicationSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18208369Submitted genomicNC_000002.12:g.237
    953314_241782040du
    p
    GRCh38 (hg38)NC_000002.12Chr2237,953,314241,782,040
    nssv18208369RemappedGoodNC_000002.11:g.238
    861956_242721455du
    p
    GRCh37.p13First PassNC_000002.11Chr2238,861,956242,721,455

    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)
    nssv18208369<0.001237864
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