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nsv6506257

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:6,988

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 134 SVs from 31 studies. See in: genome view    
    Submitted genomic58,166,517-58,173,504Question Mark
    Overlapping variant regions from other studies: 134 SVs from 31 studies. See in: genome view    
    Remapped(Score: Perfect):58,458,716-58,465,703Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6506257Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000015.10Chr1558,166,51758,173,504
    nsv6506257RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000015.9Chr1558,458,71658,465,703

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18026149deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18026149Submitted genomicNC_000015.10:g.581
    66517_58173504del
    GRCh38 (hg38)NC_000015.10Chr1558,166,51758,173,504
    nssv18026149RemappedPerfectNC_000015.9:g.5845
    8716_58465703del
    GRCh37.p13First PassNC_000015.9Chr1558,458,71658,465,703

    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)
    nssv18026149<0.001939240
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