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nsv6374112

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:12,391

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 179 SVs from 48 studies. See in: genome view    
    Submitted genomic11,059,780-11,072,170Question Mark
    Overlapping variant regions from other studies: 179 SVs from 48 studies. See in: genome view    
    Remapped(Score: Perfect):11,101,466-11,113,856Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6374112Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000003.12Chr311,059,78011,072,170
    nsv6374112RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000003.11Chr311,101,46611,113,856

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18092003deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18092003Submitted genomicNC_000003.12:g.110
    59780_11072170del
    GRCh38 (hg38)NC_000003.12Chr311,059,78011,072,170
    nssv18092003RemappedPerfectNC_000003.11:g.111
    01466_11113856del
    GRCh37.p13First PassNC_000003.11Chr311,101,46611,113,856

    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)
    nssv18092003<0.001238990
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