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nsv7070869

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:82,987

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 312 SVs from 51 studies. See in: genome view    
    Submitted genomic65,256,389-65,339,375Question Mark
    Overlapping variant regions from other studies: 312 SVs from 51 studies. See in: genome view    
    Remapped(Score: Perfect):65,290,292-65,373,278Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7070869Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000016.10Chr1665,256,38965,339,375
    nsv7070869RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000016.9Chr1665,290,29265,373,278

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18758138inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18758138Submitted genomicNC_000016.10:g.652
    56389_65339375inv
    GRCh38 (hg38)NC_000016.10Chr1665,256,38965,339,375
    nssv18758138RemappedPerfectNC_000016.9:g.6529
    0292_65373278inv
    GRCh37.p13First PassNC_000016.9Chr1665,290,29265,373,278

    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)
    nssv187581387e-062276268
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