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nsv6563073

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:4,786,318

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 12072 SVs from 120 studies. See in: genome view    
    Submitted genomic52,107,269-56,893,586Question Mark
    Overlapping variant regions from other studies: 12072 SVs from 120 studies. See in: genome view    
    Remapped(Score: Perfect):51,972,067-56,758,384Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6563073Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000006.12Chr652,107,26956,893,586
    nsv6563073RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000006.11Chr651,972,06756,758,384

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18271481inversionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18271481Submitted genomicNC_000006.12:g.521
    07269_56893586inv
    GRCh38 (hg38)NC_000006.12Chr652,107,26956,893,586
    nssv18271481RemappedPerfectNC_000006.11:g.519
    72067_56758384inv
    GRCh37.p13First PassNC_000006.11Chr651,972,06756,758,384

    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)
    nssv18271481<0.0011239304
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