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nsv6480485

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:2,500

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 80 SVs from 23 studies. See in: genome view    
    Submitted genomic70,640,601-70,643,100Question Mark
    Overlapping variant regions from other studies: 80 SVs from 23 studies. See in: genome view    
    Remapped(Score: Perfect):71,107,318-71,109,817Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6480485Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000014.9Chr1470,640,60170,643,100
    nsv6480485RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000014.8Chr1471,107,31871,109,817

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18180302duplicationSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18180302Submitted genomicNC_000014.9:g.7064
    0601_70643100dup
    GRCh38 (hg38)NC_000014.9Chr1470,640,60170,643,100
    nssv18180302RemappedPerfectNC_000014.8:g.7110
    7318_71109817dup
    GRCh37.p13First PassNC_000014.8Chr1471,107,31871,109,817

    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)
    nssv18180302<0.001136698
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