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nsv6474110

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:95,848

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 378 SVs from 49 studies. See in: genome view    
    Submitted genomic9,876,746-9,972,593Question Mark
    Overlapping variant regions from other studies: 379 SVs from 49 studies. See in: genome view    
    Remapped(Score: Perfect):10,029,345-10,125,192Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6474110Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000012.12Chr129,876,7469,972,593
    nsv6474110RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000012.11Chr1210,029,34510,125,192

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18006158deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18006158Submitted genomicNC_000012.12:g.987
    6746_9972593del
    GRCh38 (hg38)NC_000012.12Chr129,876,7469,972,593
    nssv18006158RemappedPerfectNC_000012.11:g.100
    29345_10125192del
    GRCh37.p13First PassNC_000012.11Chr1210,029,34510,125,192

    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)
    nssv18006158<0.001339234
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