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nsv6410738

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:24,144

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 197 SVs from 43 studies. See in: genome view    
    Submitted genomic68,031,756-68,055,899Question Mark
    Overlapping variant regions from other studies: 197 SVs from 43 studies. See in: genome view    
    Remapped(Score: Perfect):68,741,648-68,765,791Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6410738Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000006.12Chr668,031,75668,055,899
    nsv6410738RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000006.11Chr668,741,64868,765,791

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18147347deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18147347Submitted genomicNC_000006.12:g.680
    31756_68055899del
    GRCh38 (hg38)NC_000006.12Chr668,031,75668,055,899
    nssv18147347RemappedPerfectNC_000006.11:g.687
    41648_68765791del
    GRCh37.p13First PassNC_000006.11Chr668,741,64868,765,791

    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)
    nssv18147347<0.001139140
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