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nsv6328669

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:517

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 122 SVs from 20 studies. See in: genome view    
    Submitted genomic60,007,562-60,008,078Question Mark
    Overlapping variant regions from other studies: 122 SVs from 20 studies. See in: genome view    
    Remapped(Score: Perfect):60,473,234-60,473,750Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6328669Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr160,007,56260,008,078
    nsv6328669RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr160,473,23460,473,750

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18062034deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18062034Submitted genomicNC_000001.11:g.600
    07562_60008078del
    GRCh38 (hg38)NC_000001.11Chr160,007,56260,008,078
    nssv18062034RemappedPerfectNC_000001.10:g.604
    73234_60473750del
    GRCh37.p13First PassNC_000001.10Chr160,473,23460,473,750

    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)
    nssv18062034<0.0011138546
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