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nsv6445212

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:3,200

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 135 SVs from 37 studies. See in: genome view    
    Submitted genomic133,624,101-133,627,300Question Mark
    Overlapping variant regions from other studies: 135 SVs from 37 studies. See in: genome view    
    Remapped(Score: Perfect):135,437,605-135,440,804Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6445212Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000010.11Chr10133,624,101133,627,300
    nsv6445212RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000010.10Chr10135,437,605135,440,804

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18177171duplicationSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18177171Submitted genomicNC_000010.11:g.133
    624101_133627300du
    p
    GRCh38 (hg38)NC_000010.11Chr10133,624,101133,627,300
    nssv18177171RemappedPerfectNC_000010.10:g.135
    437605_135440804du
    p
    GRCh37.p13First PassNC_000010.10Chr10135,437,605135,440,804

    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)
    nssv18177171<0.001532716
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