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nsv6470355

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,892

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 128 SVs from 22 studies. See in: genome view    
    Submitted genomic9,903,053-9,904,944Question Mark
    Overlapping variant regions from other studies: 129 SVs from 22 studies. See in: genome view    
    Remapped(Score: Perfect):10,055,652-10,057,543Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6470355Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000012.12Chr129,903,0539,904,944
    nsv6470355RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000012.11Chr1210,055,65210,057,543

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18006166deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18006166Submitted genomicNC_000012.12:g.990
    3053_9904944del
    GRCh38 (hg38)NC_000012.12Chr129,903,0539,904,944
    nssv18006166RemappedPerfectNC_000012.11:g.100
    55652_10057543del
    GRCh37.p13First PassNC_000012.11Chr1210,055,65210,057,543

    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)
    nssv18006166<0.001139120
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