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nsv6420574

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:6,943

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 177 SVs from 22 studies. See in: genome view    
    Submitted genomic27,045,823-27,052,765Question Mark
    Overlapping variant regions from other studies: 177 SVs from 22 studies. See in: genome view    
    Remapped(Score: Perfect):26,903,340-26,910,282Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6420574Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000008.11Chr827,045,82327,052,765
    nsv6420574RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000008.10Chr826,903,34026,910,282

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18166095deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18166095Submitted genomicNC_000008.11:g.270
    45823_27052765del
    GRCh38 (hg38)NC_000008.11Chr827,045,82327,052,765
    nssv18166095RemappedPerfectNC_000008.10:g.269
    03340_26910282del
    GRCh37.p13First PassNC_000008.10Chr826,903,34026,910,282

    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)
    nssv18166095<0.001139262
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