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nsv6509666

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:5,087

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 103 SVs from 23 studies. See in: genome view    
    Submitted genomic66,325,117-66,330,203Question Mark
    Overlapping variant regions from other studies: 103 SVs from 23 studies. See in: genome view    
    Remapped(Score: Perfect):66,617,455-66,622,541Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6509666Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000015.10Chr1566,325,11766,330,203
    nsv6509666RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000015.9Chr1566,617,45566,622,541

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18025405deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18025405Submitted genomicNC_000015.10:g.663
    25117_66330203del
    GRCh38 (hg38)NC_000015.10Chr1566,325,11766,330,203
    nssv18025405RemappedPerfectNC_000015.9:g.6661
    7455_66622541del
    GRCh37.p13First PassNC_000015.9Chr1566,617,45566,622,541

    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)
    nssv18025405<0.001139246
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