nsv6494617

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:7,927

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 83 SVs from 28 studies. See in: genome view    
    Submitted genomic20,721,855-20,729,781Question Mark
    Overlapping variant regions from other studies: 83 SVs from 28 studies. See in: genome view    
    Remapped(Score: Perfect):21,190,014-21,197,940Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6494617Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000014.9Chr1420,721,85520,729,781
    nsv6494617RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000014.8Chr1421,190,01421,197,940

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18179210duplicationSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18179210Submitted genomicNC_000014.9:g.2072
    1855_20729781dup
    GRCh38 (hg38)NC_000014.9Chr1420,721,85520,729,781
    nssv18179210RemappedPerfectNC_000014.8:g.2119
    0014_21197940dup
    GRCh37.p13First PassNC_000014.8Chr1421,190,01421,197,940

    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)
    nssv18179210<0.001639224
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