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nsv7066496

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:86,946

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 317 SVs from 51 studies. See in: genome view    
    Submitted genomic65,256,542-65,343,487Question Mark
    Overlapping variant regions from other studies: 317 SVs from 51 studies. See in: genome view    
    Remapped(Score: Perfect):65,290,445-65,377,390Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7066496Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000016.10Chr1665,256,54265,343,487
    nsv7066496RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000016.9Chr1665,290,44565,377,390

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18758139inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18758139Submitted genomicNC_000016.10:g.652
    56542_65343487inv
    GRCh38 (hg38)NC_000016.10Chr1665,256,54265,343,487
    nssv18758139RemappedPerfectNC_000016.9:g.6529
    0445_65377390inv
    GRCh37.p13First PassNC_000016.9Chr1665,290,44565,377,390

    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)
    nssv187581397e-062275064
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