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nsv7045135

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:6,204

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 126 SVs from 24 studies. See in: genome view    
    Submitted genomic110,420,440-110,426,643Question Mark
    Overlapping variant regions from other studies: 126 SVs from 24 studies. See in: genome view    
    Remapped(Score: Perfect):110,741,643-110,747,846Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7045135Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000006.12Chr6110,420,440110,426,643
    nsv7045135RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000006.11Chr6110,741,643110,747,846

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18776618inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18776618Submitted genomicNC_000006.12:g.110
    420440_110426643in
    v
    GRCh38 (hg38)NC_000006.12Chr6110,420,440110,426,643
    nssv18776618RemappedPerfectNC_000006.11:g.110
    741643_110747846in
    v
    GRCh37.p13First PassNC_000006.11Chr6110,741,643110,747,846

    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)
    nssv18776618<0.00135274646
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